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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309582Generated: November 4, 2026

Pyridine → HCID 54560567, compound

https://huagongshe.com/reaction/2309582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiketeneHCID 12661—
ReactantChlorineHCID 24526—
Reactant4-Chloro-3-oxobutyryl chlorideHCID 3016262—
ReactantHCID 21400465HCID 21400465—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 54560567HCID 54560567—

Reaction Steps

In 100 ml of methylene chloride was dissolved 35.4 g (0.421 mole) of diketene. The solution was cooled to -30° to -35° C. and 29.5 g (0.415 mole) of chlorine was bubbled into the solution for about an hour to prepare 4-chloroacetoacetyl chloride. The solution was cooled to 40° C. or below and a solution of 50 g (0.324 mole) of phenylthioethanol and 25.6 g (0.324 mole) of pyridine in 52 ml of methylene chloride was added dropwise to the solution at -20° C. or below over a period of about an hour. After completion of addition, the reaction was allowed to proceed at -5° C. for about an hour. To the reaction mixture were added 400 ml of methylene chloride and 700 ml of water to extract the reaction product. The aqueous layer was further extracted with 200 ml of methylene chloride. The organic layers were combined, washed with water and concentrated to dryness under reduced pressure to give 88.5 g of phenylthioethyl 4-chloroacetoacetate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695639
Source datasetuspto-grants-1987_09
ORD IDord-0bb5cd4f7f3948acb40a1658db250ae0
Source noteuspto-grants-1987_09