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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647402Generated: October 29, 2026

Acetic Anhydride → HCID 13257591, compound

https://huagongshe.com/reaction/647402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13252412HCID 13252412—
SolventPyridineHCID 1049—
ProductHCID 13257591HCID 1325759195%

Reaction Steps

In 75 ml of pyridine was dissolved 28.2 g of 2-(4-chloro-2-fluorophenyl)-3a-hydroxy-1-thioxo-octahydroisoindole-3-one, and 30 ml of acetic acid anhydride was added to the solution, which was allowed to stand at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in dichloromethane, washed with water and dried over anhydrous sodium sulfate. After distilling off the dichloromethane, the resulting crystals were washed with a small amount of cold ethanol and dried, thereby affording 25.2 g (yield of 95%) of the subject compound. Recrystallization from ethanol yielded red-purple crystals, m.p. 101°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04409018
Source datasetuspto-grants-1983_10
ORD IDord-a96de7086dae4de6bb69246851ce0562
Source noteuspto-grants-1983_10