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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34426Generated: October 30, 2026

Oxalyl chloride → HCID 13923222, compound

https://huagongshe.com/reaction/34426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178450332HCID 178450332—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 13923222HCID 1392322284%

Reaction Steps

420 ml of oxalyl chloride were added at 0° to 5° C. to 141.2 g (0.5 mol) of 2-butyryl-3-hydroxy-5-(tetrahydrothiopyran-3-yl)cyclohex-2-en-1-one, and the mixture was stirred at room temperature for 16 hours and concentrated. The oil obtained was treated with methyl tert.-butyl ether, and the resulting solid was filtered off with suction and dried. This gave 125.9 g (84% yield) of 2-butyryl-3-chloro-5-(tetrahydrothiopyran-3-yl)cyclohex-2-en-1-one having a melting point of 97° C. (decomposition) (compound no. 312).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761486
Source datasetuspto-grants-1988_08
ORD IDord-a014d6e381fe4f1ba33060fdff7657ff
Source noteuspto-grants-1988_08