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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877188Generated: October 29, 2026

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

https://huagongshe.com/reaction/877188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl [4-(acetoxymethyl)phenyl](cyclopentyl)acetateHCID 58136319—
SolventDichloromethaneHCID 6344—
Product[4-(Acetoxymethyl)phenyl](cyclopentyl)acetic acidHCID 58136423111%

Reaction Conditions

Temperature0 °C

Reaction Steps

13.27 g (37.2 mmol, 95% pure) of tert-butyl(+/−)-{4-[(acetyloxy)methyl]phenyl}(cyclopentyl)acetate were dissolved in 117 ml of dichloromethane, the mixture was cooled to 0° C. and 58.4 ml of trifluoroacetic acid were added. The reaction mixture was initially stirred at 0° C. for 1.5 h and then at RT for a further 1.5 h. The mixture was then concentrated under reduced pressure and the residue was dried under high vacuum. The residue was taken up in 50 ml of dichloromethane, and the solution was washed four times with water. The organic phase was dried over magnesium sulfate and concentrated under reduced pressure. Drying under high vacuum gave 11.41 g of the title compound which were used without further purification for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987256B2
Source datasetuspto-grants-2015_03
ORD IDord-85362638eb3d43feafcd2d3360908f10
Source noteuspto-grants-2015_03