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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987062Generated: October 30, 2026

Trifluoroacetic acid → HCID 54195265, compound

https://huagongshe.com/reaction/987062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69301956HCID 69301956—
SolventDichloromethaneHCID 6344—
ProductHCID 54195265HCID 54195265—

Reaction Steps

To a stirred solution of 200 mg (0.32 mmol) 2-methyl-butyric acid 8-[6-benzylcarbamoyl-5-(tert.-butyl-dimethyl-silanyloxy)-3-oxo-hexyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydro-naphthalen-1-yl ester in 5 ml methylene chloride are added 0.3 g (2.6 mmol) trifluoroacetic acid. After 2 hours at room temperature the reaction mixture is quenched with saturated aqeous sodium bicarbonate. The aqueous phase is separated and extracted twice with ethyl acetate. The combined organic phases are dried over sodium sulfate and the solvent is evaporated. The residue is chromatographed over silica gel (hexane/ethyl acetate 7/3 to 2/3) affording the title compound as a white powder foam. MS (FAB) m/z 480 ([M+Li]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630492B1
Source datasetuspto-grants-2003_10
ORD IDord-38c51f0795fb44a386de423798e9a7f7
Source noteuspto-grants-2003_10