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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309575Generated: October 27, 2026

Diketene → 2-(Methanesulfonyl)ethyl 4-chloro-3-oxobutanoate

https://huagongshe.com/reaction/2309575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiketeneHCID 12661—
ReactantChlorineHCID 24526—
Reactant4-Chloro-3-oxobutyryl chlorideHCID 3016262—
ReactantMethanesulfonylethanolHCID 21979976—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product2-(Methanesulfonyl)ethyl 4-chloro-3-oxobutanoateHCID 5432407780%

Reaction Conditions

Temperature-35 °C

Reaction Steps

In 260 ml of methylene chloride was dissolved 87.9 g (1.407 moles) of diketene. The solution was cooled to -35° C. and 74.2 g (1.045 moles) of chlorine gas was bubbled into the solution at -35° to -30° C. for about 2 hours to prepare a methylene chloride solution of 4-chloroacetoacetyl chloride. Separately, 100 g (0.805 mole) of methylsulfonylethanol was dissolved in 130 ml of methylene chloride followed by addition of 63.7 g of pyridine. To this solution was added the above methylene chloride solution of 4-chloroacetoacetyl chloride at -5° to 0° C. dropwise over a period of about 1.5 hours. The mixture was then stirred for 30 minutes and poured in water, and 800 ml of methylene chloride was added to extract the reaction product. The water layer was further extracted with methylene chloride and the organic layers were combined and washed with water. The organic solution was concentrated to dryness and the concentrate was dissolved in 50 ml of methylene chloride and crystallized by addition of 200 ml of isopropyl ether to give 156.3 g (yield: 80% based on methylsulfonylethanol) of methylsulfonylethyl 4-chloroacetoacetate as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695639
Source datasetuspto-grants-1987_09
ORD IDord-5909eeb933ff449ba4fadb021813c871
Source noteuspto-grants-1987_09