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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309581Generated: November 1, 2026

Pyridine → Methylthioethyl 4-chloroacetoacetate

https://huagongshe.com/reaction/2309581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiketeneHCID 12661—
ReactantChlorineHCID 24526—
Reactant4-Chloro-3-oxobutyryl chlorideHCID 3016262—
Reactant1-(Methylthio)ethanolHCID 18425401—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethylthioethyl 4-chloroacetoacetateHCID 53866428—

Reaction Steps

In 1.26 liters of methylene chloride was dissolved 420 g (5.0 moles) of diketene. The solution was cooled at -30° to -35° C. and 354 g (4.99 moles) of chlorine gas was bubbled into the solution for about an hour to prepare a 4-chloroacetoacetyl chloride solution. 244 ml of this solution (4-chloroacetoacetyl chloride: 109.2 g, 0.705 mole) was cooled to -30° to -40° C. and a solution of 50 g (0.543 mole) of methylthioethanol and 43 g (0.543 mole) of pyridine in 85 ml of methylene chloride was added dropwise at -20° to -30° C. over a period of about 30 minutes. After completion of addition, the reaction was allowed to proceed at -5° C. for 30 minutes. To the reaction mixture were added 500 ml of methylene chloride and 1 liter of water to extract the reaction product. The aqueous layer was further extracted with 500 ml of methylene chloride. The organic layers were combined, washed with 500 ml of water and concentrated to dryness under reduced pressure to give 114 g of methylthioethyl 4-chloroacetoacetate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695639
Source datasetuspto-grants-1987_09
ORD IDord-77107065240442fd95779a2508f490fa
Source noteuspto-grants-1987_09