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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079008Generated: October 30, 2026

Citric Acid → (RS)-2-methyl-4-methylidene-3-ethyl-2-cyclopenten-1-yl (1R)-trans-3-(2,2-dichloro-vinyl)-2,2-dimethylcyclopropanecarboxylate

https://huagongshe.com/reaction/1079008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantPyridineHCID 1049—
Reactant(1R,3S)-3-(2,2-Dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chlorideHCID 6454308—
Reactant(RS)-2-methyl-4-methylidene-3-ethylcyclopent-2-en-1-olHCID 15389976—
Catalyst2,6-Di-tert-butyl-4-methylphenolHCID 31404—
SolventTolueneHCID 1140—
Product(RS)-2-methyl-4-methylidene-3-ethyl-2-cyclopenten-1-yl (1R)-trans-3-(2,2-dichloro-vinyl)-2,2-dimethylcyclopropanecarboxylateHCID 1538998286.3%

Reaction Steps

625 mg of (1R)-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid chloride was added under ice-water cooling to a mixed solution of 400 mg of (RS)-2-methyl-4-methylidene-3-ethylcyclopent-2-en-1-ol, 5 mg of 2,6-di-t-butyl-4-methylphenol and 274 mg of pyridine in 6 ml of toluene. The reaction was continued at an ambient temperature for eight hours. The reaction solution was added to a 5% citric acid solution under ice-water cooling, and extracted three times with diethyl ether. The combined ether layer was washed successively with a saturated sodium hydrogencarbonate solution and a saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. After removal of the solvent under reduced pressure, the residue was subjected to silica gel column chromatography to yield 781 mg of (RS)-2-methyl-4-methylidene-3-ethyl-2-cyclopenten-1-yl (1R)-trans-3-(2,2-dichloro-vinyl)-2,2-dimethylcyclopropanecarboxylate (Compound No.5). Yield 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550258
Source datasetuspto-grants-1996_08
ORD IDord-b9ef4c02bdbc4a6299cc4b6b2c6b5a55
Source noteuspto-grants-1996_08