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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657718Generated: October 26, 2026

Water → Tert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoate

https://huagongshe.com/reaction/1657718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
ReactantCyclopentyl methyl ketoneHCID 22326—
Reactant1,1-Dimethylethyl dichloroacetateHCID 3016483—
SolventTetrahydrofuranHCID 8028—
ProductTert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoateHCID 21443888—

Reaction Conditions

Temperature-30 °C

Reaction Steps

A mixture of 12.3 g of cyclopentylmethyl ketone and 18.5 g of tert.-butyl dichloroacetate was cooled to -30°C with stirring under an inert atmosphere and a solution of 12.2 g of potassium tert.butylate in 60 ml of tetrahydrofuran was added thereto at the said temperature. After returning to room temperature, hexane and water were added and the organic phase was separated, washed with water and dried over magnesium sulfate. The solvents were evaporated off to leave an oily residue of tert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoate. 26.5 g of the latter product were added to a solution of 3 g of lithium carbonate and 20 g of lithium bromide in 100 ml of hexamethylphosphorotriamide and after stirring for 1 hour at room temperature, petroleum ether and water were added thereto. The organic phase was washed with water, dried over magnesium sulfate and filtered. The solvent was evaporated to obtain an oily residue which was tert. butyl 3-cyclopentyl-2-oxo-3-butenoate which was used as is for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962223
Source datasetuspto-grants-1976_06
ORD IDord-f95135942e3443faaa8ed41d226b279f
Source noteuspto-grants-1976_06