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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381230Generated: October 31, 2026

Trifluoromethanesulfonic acid → Methyl (S)-3-benzyloxybutyrate

https://huagongshe.com/reaction/381230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantBenzyl 2,2,2-trichloroacetimidateHCID 144968—
ReactantMethyl 3-hydroxybutyrate, (S)-HCID 6950307—
SolventDichloromethane cyclohexaneHCID 21916607—
ProductMethyl (S)-3-benzyloxybutyrateHCID 13967615—

Reaction Steps

Methyl (S)-(+)-3-hydroxybutyrate (17) (2.223 g, 18.82 mmol) and benzyl 2,2,2-trichloroacetimidate (4.2 mL) were dissolved into 37.5 mL of cyclohexane/methylene chloride (2:1). After the addition of 0.2 mL of trifluoromethane sulfonic acid the reaction was stirred under nitrogen for one hour. The reaction was diluted with 75 mL of cyclohexane/methylene chloride (2:1) and filtered. The organic layer was washed with 50 mL of saturated sodium bicarbonate and 50 mL of distilled water. After drying with anhydrous sodium sulfate the solution was filtered and the solvents were removed on a rotovap. The resulting solid was purified using silica gel and elution with ether/hexane (1:4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306828B1
Source datasetuspto-grants-2001_10
ORD IDord-2dcfd35ef9884360bb841b2fe3e22f0b
Source noteuspto-grants-2001_10