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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492083Generated: October 30, 2026

Potassium Hydroxide → HCID 67823835, compound

https://huagongshe.com/reaction/1492083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantPotassiumHCID 5462222—
ReactantEthyl 2,2-dibromo-1,3-dimethylcyclopropane-1-carboxylateHCID 12406051—
ReactantMethyl 2-[2-(bromomethyl)phenyl]-3-methoxyprop-2-enoateHCID 53395349—
ReactantHCID 131718792HCID 131718792—
SolventEthanolHCID 702—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67823835HCID 6782383532%

Reaction Steps

A solution of 11.0 g (36 mmol) of ethyl 1,2-dimethyl-3,3-dibromocyclopropanecarboxylate (prepared according to Intermediate 12a) and 2.2 g (40 mmol) of potassium hydroxide in 100 ml of ethanol was stirred for 6 hours at 60° C. and then evaporated down. The solution was covered with a layer of diethyl ether, after which the resulting precipitate was separated off and washed with diethyl ether. Subsequent reaction of the resulting potassium salt of dimethyldibromocyclopropanecarboxylic acid in 60 ml of N-methylpyrrolidone with 5.1 g (18 mmol) of methyl alpha- (2-bromomethylphenyl ) -beta-methoxyacrylate was carried out similarly to Example 1. After hydrolysis of the reaction mixture, the product was extracted with methyl tert-butyl ether and was isolated and purified similarly to Example 1. Yield: 32% colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371268
Source datasetuspto-grants-1994_12
ORD IDord-bf5545f52c904817a2b8dda34759200b
Source noteuspto-grants-1994_12