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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440385Generated: October 31, 2026

Cyclopropanecarbonyl chloride → 73252-24-1

https://huagongshe.com/reaction/1440385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantEthyl isocyanoacetateHCID 533707—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product73252-24-1HCID 13496996—

Reaction Steps

A mixture of ethyl isocyanoacetate (13.4 g) in THF (65 ml) was added dropwise to a stirred solution of potassium tert-butoxide (14.5 g) in THF (97 ml) at 0° C. Cyclopropanecarboxylic acid chloride (5.4 ml) was added dropwise at below 10° C. and the solvent evaporated. Water (68 ml) and acetic acid (3.4 ml) was added to the mixture, then diisopropyl ether (2×150 ml) was added and the layers separated. The aqueous layer was further extracted with diisopropyl ether (2×150 ml) and the combined organic extracts were dried. Evaporation of the solvent afforded the title compound as a yellow oil (8.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498722
Source datasetuspto-grants-1996_03
ORD IDord-252c4f225fbc4d19a2c4f2f5b796d6cd
Source noteuspto-grants-1996_03