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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475645Generated: October 30, 2026

Trifluoroacetic acid → [4-(Acetoxymethyl)phenyl](cyclopentyl)acetic acid

https://huagongshe.com/reaction/1475645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl [4-(acetoxymethyl)phenyl](cyclopentyl)acetateHCID 58136319—
SolventDichloromethaneHCID 6344—
Product[4-(Acetoxymethyl)phenyl](cyclopentyl)acetic acidHCID 5813642391%

Reaction Conditions

Temperature0 °C

Reaction Steps

11.70 g (35.19 mmol) of tert-butyl [4-(acetoxymethyl)phenyl](cyclopentyl)acetate were dissolved in 108.5 ml of dichloromethane, the mixture was cooled to 0° C. and 39.2 ml of trifluoroacetic acid were added. The reaction mixture was stirred first at 0° C. for 1.5 h and then at RT for 1.5 h and then concentrated under reduced pressure. The residue was taken up in 50 ml of dichloromethane and the solution was washed four times with in each case 30 ml of water. The organic phase was dried over magnesium sulphate and concentrated under reduced pressure and the residue was dried under high vacuum. This gave 9.83 g of the target compound as a crude product (about 90% pure, yield 91% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018258B2
Source datasetuspto-grants-2015_04
ORD IDord-a6fd8cf477c248f08935d033f318fe38
Source noteuspto-grants-2015_04