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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987057Generated: October 30, 2026

Trifluoromethanesulfonic anhydride → HCID 54052594, compound

https://huagongshe.com/reaction/987057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 20678451HCID 20678451—
SolventDichloromethaneHCID 6344—
ProductHCID 54052594HCID 54052594—

Reaction Steps

To a cooled (−77° C.) solution of 73 mg (0.18 mmol) of 2-methyl-butyric acid 3,7-dimethyl-8-(3,5,7-trihydroxy-heptyl)-1,2,3,7,8,8a-hexahydro-naphthalen-1-yl ester in 5 ml of methylene chloride is added 0.9 g (7 mmol) Hunig's base and 0.08 ml (0.5 mmol) triflic anhydride. After 30 minutes the reaction is quenched with saturated aqueous sodium bicarbonate. The phases are separated and the water phase is extracted twice with ethyl acetate. The organic phases are combined, washed with brine and dried over sodium sulfate. The solvent is evaporated and the crude product is purified by silica gel chromatography (diethyl ether/hexane 1/4) to afford the desired product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630492B1
Source datasetuspto-grants-2003_10
ORD IDord-30db6072d4bf45dcb20f58df83e5b3d3
Source noteuspto-grants-2003_10