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All posts Subject: TRIETHYLOXONIUM FLUOBORATE Please login to post

zealot
(Мастер)
10-27-03 17:40
No 467042
User Picture TRIETHYLOXONIUM FLUOBORATE

1. Procedure
A 2-1. three-necked flask, a stirrer, a dropping funnel, and a condenser provided with a drying tube are dried in an oven at 110°, assembled while hot, and cooled in a stream of dry nitrogen. Sodium-dried ether (500 ml.) and 284 g. (252 ml., 2.00 moles) of freshly distilled boron fluoride etherate (Notes 1 and 2) are placed in the flask. Epichlorohydrin (140 g., 119 ml., 1.51 moles) is added dropwise to the stirred solution at a rate sufficient to maintain vigorous boiling (about 1 hour is needed). The mixture is refluxed an additional hour and allowed to stand at room temperature overnight. The stirrer is replaced by a filter stick, and the supernatant ether is withdrawn from the crystalline mass of triethyloxonium fluoborate; nitrogen is admitted through a bubbler during this operation to prevent atmospheric moisture from entering the flask. The crystals are washed with three 500-ml. portions of sodium-dried ether. The flask is transferred to a dry box, and triethyloxonium fluoborate is collected on a sintered-glass filter and bottled in a stream of dry nitrogen. The fluoborate is colorless; m.p. 91-92° (dec.), yield 244-272 g. (85-95%) (Note 3).

2. Notes
1. The checkers obtained boron fluoride etherate and epichloro-hydrin from Eastman Organic Chemicals and redistilled each through a 23-cm. Vigreux column immediately before use.
2. It is convenient to measure the liquids with syringes using the densities: epichlorohydrin d25_4 1.179; boron fluoride etherate, d25_4 1.125.
3. Triethyloxonium fluoborate is very hygroscopic. It should be stored in a tightly closed screw-cap bottle at 0-5° and should be used within a few days of the time it is made. It should be weighed and transferred in a dry box. It can be stored indefinitely under ether or at —80°.

3. Methods of Preparation
The procedure used is essentially that described by Meerwein and co-workers.2'' The salt also has been prepared from ethyl fluoride and boron fluoride etherate, and from silver fluoborate, ethyl bromide, and ether.4

4. Merits of the Preparation
This simple procedure easily provides large amounts of tri-ethyloxonium fluoborate. Triethyloxonium fluoborate readily ethylates such compounds as ethers, sulfides, nitriles, ketones, esters, and amides on oxygen, nitrogen, or sulfur to give onium fluoborates (often isolable) that can react with nucleophilic reagents to give useful products.6 For example, dimethylforma-mide gives the imino ether fluoborate [(CH3)2NCH—OC2H5]+ BF4-, which is converted to (CH3)2NCH(OC2H5)2 by sodium ethoxide.5 Since an imino ether fluoborate is easily hydrolyzed to the corresponding amine and ester, triethyloxonium fluoborate is a useful reagent for converting amides to amines under mild conditions.8
If there is no advantage in ethylation over methylation, tri-methyloxonium fluoborate6 or trimethyloxonium 2,4,6-trinitro-benzenesulfonate7 may be preferable alkylating agents; their
preparation is more laborious, but they may be stored for a longer period of time.

1. Deceased October 24, 1965; formerly at University of Marburg, Marburg, Germany.
2. H. Meerwein, E. Bettenberg, H. Gold, E. Pfeil, and G. Willfang, 7. Prakt. Chem., [2] 154, 83 (1940).
3. H. Meerwein, G. Hinz, P. Hofmann, E. Kroning, and E. Pfeil, J. Prakt. Ckem., [2] 14;, 257 (1937).
4. H. Meerwein, V. Hederich, and K. Wunderlich, Arch. Pharm., 291, 552 (1958).
5. H. Meerwein, P. Borner, 0. Fuchs, H. J. Sasse, H. Schrodt, and J. Spille, Ber.,
89, 2060 (1956). 0. H. Meerwein, Org. Syntheses, this volume, p. 120.
7. G. K. Helmkamp and D. J. Pettitt, Org. Syntheses, this volume, p. 122.
8. H. Muxfeldt and W. Rogalski, J. Am. Chem. Sue., 87, 933 (1965).

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		zealot (Мастер) 10-27-03 17:40 No 467042				TRIETHYLOXONIUM FLUOBORATE
						1. Procedure A 2-1. three-necked flask, a stirrer, a dropping funnel, and a condenser provided with a drying tube are dried in an oven at 110°, assembled while hot, and cooled in a stream of dry nitrogen. Sodium-dried ether (500 ml.) and 284 g. (252 ml., 2.00 moles) of freshly distilled boron fluoride etherate (Notes 1 and 2) are placed in the flask. Epichlorohydrin (140 g., 119 ml., 1.51 moles) is added dropwise to the stirred solution at a rate sufficient to maintain vigorous boiling (about 1 hour is needed). The mixture is refluxed an additional hour and allowed to stand at room temperature overnight. The stirrer is replaced by a filter stick, and the supernatant ether is withdrawn from the crystalline mass of triethyloxonium fluoborate; nitrogen is admitted through a bubbler during this operation to prevent atmospheric moisture from entering the flask. The crystals are washed with three 500-ml. portions of sodium-dried ether. The flask is transferred to a dry box, and triethyloxonium fluoborate is collected on a sintered-glass filter and bottled in a stream of dry nitrogen. The fluoborate is colorless; m.p. 91-92° (dec.), yield 244-272 g. (85-95%) (Note 3). 2. Notes 1. The checkers obtained boron fluoride etherate and epichloro-hydrin from Eastman Organic Chemicals and redistilled each through a 23-cm. Vigreux column immediately before use. 2. It is convenient to measure the liquids with syringes using the densities: epichlorohydrin d25_4 1.179; boron fluoride etherate, d25_4 1.125. 3. Triethyloxonium fluoborate is very hygroscopic. It should be stored in a tightly closed screw-cap bottle at 0-5° and should be used within a few days of the time it is made. It should be weighed and transferred in a dry box. It can be stored indefinitely under ether or at —80°. 3. Methods of Preparation The procedure used is essentially that described by Meerwein and co-workers.2'' The salt also has been prepared from ethyl fluoride and boron fluoride etherate, and from silver fluoborate, ethyl bromide, and ether.4 4. Merits of the Preparation This simple procedure easily provides large amounts of tri-ethyloxonium fluoborate. Triethyloxonium fluoborate readily ethylates such compounds as ethers, sulfides, nitriles, ketones, esters, and amides on oxygen, nitrogen, or sulfur to give onium fluoborates (often isolable) that can react with nucleophilic reagents to give useful products.6 For example, dimethylforma-mide gives the imino ether fluoborate [(CH3)2NCH—OC2H5]+ BF4-, which is converted to (CH3)2NCH(OC2H5)2 by sodium ethoxide.5 Since an imino ether fluoborate is easily hydrolyzed to the corresponding amine and ester, triethyloxonium fluoborate is a useful reagent for converting amides to amines under mild conditions.8 If there is no advantage in ethylation over methylation, tri-methyloxonium fluoborate6 or trimethyloxonium 2,4,6-trinitro-benzenesulfonate7 may be preferable alkylating agents; their preparation is more laborious, but they may be stored for a longer period of time. 1. Deceased October 24, 1965; formerly at University of Marburg, Marburg, Germany. 2. H. Meerwein, E. Bettenberg, H. Gold, E. Pfeil, and G. Willfang, 7. Prakt. Chem., [2] 154, 83 (1940). 3. H. Meerwein, G. Hinz, P. Hofmann, E. Kroning, and E. Pfeil, J. Prakt. Ckem., [2] 14;, 257 (1937). 4. H. Meerwein, V. Hederich, and K. Wunderlich, Arch. Pharm., 291, 552 (1958). 5. H. Meerwein, P. Borner, 0. Fuchs, H. J. Sasse, H. Schrodt, and J. Spille, Ber., 89, 2060 (1956). 0. H. Meerwein, Org. Syntheses, this volume, p. 120. 7. G. K. Helmkamp and D. J. Pettitt, Org. Syntheses, this volume, p. 122. 8. H. Muxfeldt and W. Rogalski, J. Am. Chem. Sue., 87, 933 (1965).

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