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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851683Generated: October 29, 2026

Acetic Anhydride → HCID 13051756, compound

https://huagongshe.com/reaction/851683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 12902576HCID 12902576—
ProductHCID 13051756HCID 1305175643%

Reaction Steps

314.6 g (1 mol) of 1,1,1-trichloro-2-hydroxy-3-(1,2,4-triazol-1-yl)-5,5-dimethyl-hexan-4-one were heated at 95° C. in 1,000 ml of acetic anhydride for 30 hours. The excess anhydride was then distilled off in vacuo, the residue was taken up in 750 ml of methylene chloride and the methylene chloride mixture was washed with 10% strength sodium bicarbonate solution until neutral. The organic phase was dried over sodium sulphate and concentrated by distilling off the solvent in vacuo. The residue was stirred with 150 ml of diisopropyl ether. 153.8 g (43% of theory) of 1,1,1-trichloro-2-acetoxy-3-(1,2,4-triazol-1-yl)-5,5-dimethyl-hexan-4-one were obtained as the pure diastereomer of the A* form of melting point 129°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04386088
Source datasetuspto-grants-1983_05
ORD IDord-3564c141f7e04734a6c4441b275f9a76
Source noteuspto-grants-1983_05