U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Difluoromethyl ether derivative and process for producing the same

Patent 6864397 Issued on March 8, 2005. Estimated Expiration Date: Icon_subject June 18, 2023. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Trifluorobenzene derivative and liquid crystal composition containing the same
Patent #: 5032313
Issued on: 07/16/1991
Inventor: Goto, et al.

Difluoromethylene compounds
Patent #: 5045229
Issued on: 09/03/1991
Inventor: Bartmann, et al.

Polyhaloalkyl ether derivatives as well as liquid crystal compositions and liquid crystal display elements containing them Patent #: 6007740
Issued on: 12/28/1999
Inventor: Andou, et al.

Inventors

Assignee

Application

No. 10463616 filed on 06/18/2003

US Classes:

568/647, Halogen containing568/631, Plural rings containing568/640, Plural benzene rings bonded directly to the same carbon568/641, Polyoxy and halogen containing568/642, Plural benzene rings bonded directly to each other568/643, Polyoxy568/645, Halogen containing568/646Acyclic carbon to carbon unsaturation containing

Examiners

Primary: Keys, Rosalynd

Attorney, Agent or Firm

Foreign Patent References

  • 2-233626 JP 09/01/1990
  • 5-112778 JP 05/01/1993
  • 5-255165 JP 10/01/1993

International Classes

C07C041/06
C07C025/18
C09K019/20
C07C043/12

Abstract

The present invention provides a process for producing a difluoromethyl ether derivative simple and efficient process for producing the difluoromethyl ether derivative represented by Formula (1d′) or a difluoromethyl ether derivative represented by Formula (1c′): wherein all the variables are defined in the specification.

Other References

  • Abstract of JP 10204016.
  • Hayashi, S., et al. “Convenient Procedures for Conversion of Carbonyl Compounds to gem -Difluoroolefins and Their Selective Reductions to Monofluoroolefins”, Chemistry Letters, 1979, pp. 983-986.
  • Haas, A., et al. “Synthese seitenkettenfluorierter aromatischer Verbindungen und deren Chemische Reaktivitat”, Chem. Ber., vol. 121 (1988), pp. 1329-1340.
  • Kirsch et al., “Liquid Crystals with multiple flourinated bridges in the mesogenic core structure”, Journal of Fluorine Chemistry, vol. 112, No. 1, pp. 69-72, 2001.
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