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US4157344A Expired / Lapsed US ⏱️ 0.0 years remaining

Preparation of aryl trifluoromethyl ethers

Assignee: EIDP Inc
•
Filing: 1978-01-16
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Granted: 1979-06-05
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Expires: 1998-01-16
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Abstract

Abstract A one-step process for the synthesis of aryl trifluoromethyl ethers by reacting phenol or certain substituted phenols with a perhalomethane and hydrogen fluoride is provided. The compounds produced by the process of this invention are useful intermediates in the production of dyestuffs and pharmaceuticals.

Inventors

  • 👤 Andrew E. Feiring

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 03:34
CPC Classifications
C; C07; C07C; C07C41/00; C07C41/01; C07C41/16; C07C201/00; C07C201/06; C07C201/12; C07C213/00; C07C213/06; C07C253/00; C07C253/30; C07C45/00; C07C45/61; C07C45/67; C07C45/68; C07C45/70; C07C45/71

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 149 words
The process of preparing an aryl trifluoromethyl ether of the general formula: ##STR22## comprising reacting in the temperature range of about 80° to about 175° C. and under sufficient pressure to keep most of the hydrogen fluoride in the liquid state the following: (a) a phenolic compound of the formula ##STR23## wherein, independently, R is H, Cl, F or Br; R 1 is H, Cl, Br, F, NO 2 , NH 2 , CN, CF 3 , alkyl containing 1-4 carbon atoms, phenyl or benzoyl; and R 2 is H, Cl, Br, F, NO 2 , NH 2 , CN, CF 3 , alkyl containing 1-4 carbon atoms, phenyl, benzoyl or OH; and (b) at least an equimolar amount of a perhalomethane selected from the group consisting of CCl 4 , CFCl 3 or CBrCl 3 ; and (c) at least three molar equivalents of substantially anhydrous hydrogen fluoride.
Claim 2
Dependent Claim 149 words
The process of preparing an aryl trifluoromethyl ether of the general formula: ##STR22## comprising reacting in the temperature range of about 80° to about 175° C. and under sufficient pressure to keep most of the hydrogen fluoride in the liquid state the following: (a) a phenolic compound of the formula ##STR23## wherein, independently, R is H, Cl, F or Br; R 1 is H, Cl, Br, F, NO 2 , NH 2 , CN, CF 3 , alkyl containing 1-4 carbon atoms, phenyl or benzoyl; and R 2 is H, Cl, Br, F, NO 2 , NH 2 , CN, CF 3 , alkyl containing 1-4 carbon atoms, phenyl, benzoyl or OH; and (b) at least an equimolar amount of a perhalomethane selected from the group consisting of CCl 4 , CFCl 3 or CBrCl 3 ; and (c) at least three molar equivalents of substantially anhydrous hydrogen fluoride.
Claim 3
Dependent Claim 60 words
The process of claim 1 wherein (a) the phenolic compound is reacted with (b) the perhalomethane being present in an amount 2-3 moles per mole of phenolic compound, and (c) from 20-45 moles of substantially anhydrous hydrogen fluoride per mole of phenolic compound, the reaction being carried out in the temperature range of 125° to 150° C. under autogenous pressure.
Claim 4
Dependent Claim 27 words
The process of claim 2 wherein said phenolic compound is selected from the group 3-nitrophenol, 4-nitrophenol, 4-chlorophenol, 4-aminophenol, or 2,4-dichlorophenol and the perhalomethane is CCl 4 .

References Cited (Backward Citations)

GB765527A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-06-04 1982-12-04 1983-06-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-06-04 1986-12-04 1987-06-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-06-04 1990-12-04 1991-06-05 $7700.00 Window Closed / Lapsed

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