Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980209Generated: October 31, 2026

Hydrochloric Acid → HCID 53662515, compound

https://huagongshe.com/reaction/1980209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant(4-Fluoro-3-phenoxyphenyl)methanolHCID 12874224—
Reactant2,2-Dimethyl-3-(2-methyl-2-(4-chlorophenyl)-vinyl)-cyclopropanecarboxylic acid chlorideHCID 54483640—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 53662515HCID 5366251574.9%

Reaction Steps

5.4 g (0.025 mol) of 3-phenoxy-4-fluoro-benzyl alcohol and 7 g (0.025 mol) of 2,2-dimethyl-3-(2-methyl-2-(4-chlorophenyl)-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. Stirring was then continued at 25°-35° C. for a further 3 hours. The reaction mixture was poured into 150 ml of water, to which 5 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 residues of solvent were removed by brief incipient distillation at a bath temperature of 60° C./1 mm Hg. 8.7 g (74.9% of theory) of 2,2-dimethyl-3-(2-methyl-2-(4-chlorophenyl)-vinyl)-cyclopropane-carboxylic acid 3-phenoxy-4-fluoro-benzyl ester were obtained as a yellow viscous oil with the refractive index nD23 : 1.5735.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04485252
Source datasetuspto-grants-1984_11
ORD IDord-8453b44a9b174e658b88f4696e8b087c
Source noteuspto-grants-1984_11