Preparation of halofluoroalkyl ethers

Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing

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568683, 568669, 568684, 568685, C07C 4116

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044232497

ABSTRACT:
Alkyl or aryl 1,1-difluoroalkyl ethers, e.g., 1,1,2-trifluoro-2-chloro-2-iodoethyl phenyl ether, are prepared by reacting an alkoxide or phenoxide with a 1,1-difluoro-1,2-dihaloethane (with the proviso that halo is not fluoro and at least one of the halo substituents is bromo or iodo) in an organic solvent at temperatures ranging from about -30.degree. C. to about 100.degree. C. These compounds may be dehalogenated with zinc to form the corresponding vinyl ethers.
The reaction of halogen derivatives of fluorocarbons with nucleophiles is dramatically facilitated by a bromo or iodo substituent in the beta position.

REFERENCES:
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patent: 4377711 (1983-03-01), Rico et al.
Tarrant et al., J.A.C.S., vol. 75 (1953) 932-934.
Corley et al., J.A.C.S., vol. 78 (1956) 3489-3493.
Scipioni et al., (English Translation) Ann. Chim. Rome, 57(7) (1967) 817-824.
Banus et al., J. Chem. Soc. (1951) 60-64.

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