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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435184Generated: October 30, 2026

Hydrochloric Acid → HCID 54160409, compound

https://huagongshe.com/reaction/435184

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., while stirring. The mixture was then stirred at 25°-35° C. for a further 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 under a waterpump vacuum. Last residues of solvent were removed by brief incipient distillation at a bath temperature of 60° C./1 mm Hg. 8.1 g (84.5% of theory) of 2,2-dimethyl-3-(2-chloro-2-(4-methoxyphenyl)-vinyl)-cyclopropanecarboxylic acid (4-fluoro-3-phenoxy-benzyl)-ester were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04400523
Source datasetuspto-grants-1983_08
ORD IDord-2dcefe63d57241dfb5776b7b730b8c67
Source noteuspto-grants-1983_08