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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987059Generated: October 30, 2026

Acetic Anhydride → HCID 25029024, compound

https://huagongshe.com/reaction/987059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantLovastatinHCID 53232—
SolventPyridineHCID 1049—
ProductHCID 25029024HCID 25029024—

Reaction Steps

To a stirred solution of 4.0 g (10 mmol) mevinolin in 20 ml pyridine at room temperature are added 20 ml acetic acid anhydride. After 1 h the reaction mixture is concentrated in-vacuo. The residue is dissolved with 10 ml methyl-t-butyl ether and washed successively with water, 0.1 N HCl and brine. The organic phase is then dried over sodium sulfate and the solvent removed in vacuo. The crude product is purified by silica gel chromatography (methyl-t-butyl ether 1/3) to afford 2-methyl-butyric acid 3,7-dimethyl-8-[2-(6-oxo-3,6-dihydro-2H-pyran-2-yl)-ethyl]-1,2,3,7,8,8a-hexahydro-naphthalen-1-yl ester) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630492B1
Source datasetuspto-grants-2003_10
ORD IDord-ab039fd5714746cd8e15915e339505f7
Source noteuspto-grants-2003_10