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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286154Generated: October 30, 2026

Hydrochloric Acid → HCID 54160409, compound

https://huagongshe.com/reaction/2286154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant(4-Fluoro-3-phenoxyphenyl)methanolHCID 12874224—
ReactantHCID 53893220HCID 53893220—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 54160409HCID 5416040984.5%

Reaction Steps

4.4 g (0.02 mol) of 3-phenoxy-4-fluoro-benzyl alcohol and 7.1 g (0.02 mol) of 2,2-dimethyl-3-(2-chloro-2-(4-methoxy-phenyl)-vinyl)-cyclopropanecarboxylic acid chloride were dissolved in 100 ml of anhydrous toluene, and 2.5 g of pyridine, dissolved in 50 ml of anhydrous toluene, were added dropwise at 20°-25° C., whilst stirring. Stirring was then continued at 25°-35° C. for 3 hours. The reaction mixture was poured into 150 ml of water, to which 10 ml of concentrated hydrochloric acid were added, and the organic phase was separated off and washed again with 100 ml of water. The toluene phase was then dried over sodium sulphate and the solvent was distilled off under a water-pump vacuum. Last solvent residues were removed by brief incipient distillation at a bath temperature of 60° C./1 Hg. 8.1 g (84.5% of theory) of 2,2-dimethyl-3-(2-chloro-2-(4-methoxy-phenyl)-vinyl)-cyclopropanecarboxylic acid 4-fluoro-3-phenoxy-benzyl ester were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04327025
Source datasetuspto-grants-1982_04
ORD IDord-30b7564202424c47b6b21cdeb6e56757
Source noteuspto-grants-1982_04