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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371727Generated: October 31, 2026

Phosgene → 3-[2-Fluoro-5-(trifluoromethyl)phenoxy]-1-azetidinecarbonyl chloride

https://huagongshe.com/reaction/2371727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Diphenylmethyl)-3-[2-fluoro-5-(trifluoromethyl)phenoxy]azetidineHCID 19906227—
SolventDichloromethaneHCID 6344—
Product3-[2-Fluoro-5-(trifluoromethyl)phenoxy]-1-azetidinecarbonyl chlorideHCID 15042233163.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 10.8 g (0.11 mole) of phosgene and 14.2 g (0.11 mole) of potassium carbonate in 200 mL of methylene chloride was cooled to 5° C. in an ice bath while stirring undr nitrogen. After 30 min, the reaction mixture was treated with 40 g (0.1 mole) of 1-(diphenylmethyl)-3-[2-fluoro-5-(trifluoromethyl)phenoxy]azetidine in 100 mL of methylene chloride added dropwise. After stirring for 16 h, the reaction mixture was treated with small pieces of ice to destroy any excess phosgene. Then the reaction mixture was decanted from the inorganic paste and concentrated in vacuo to give 48.6 g of pale yellow oil. The residual oil was distilled at 0.15 mmHg to yield 3 fractions: #1, 12.7 g at 120°-128°; #2, 1.5 g at 128°, and #3 at 128°-132°; with total yield of 19.7 g (66.2%). A sample of fraction #2 was submitted for analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05095014
Source datasetuspto-grants-1992_03
ORD IDord-1f2211643d4d4312b70bea3b5be5d3b9
Source noteuspto-grants-1992_03