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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877193Generated: October 30, 2026

Sulfuric Acid → tert-Butyl(2S)-cyclopentyl-(4-methylphenyl)acetate

https://huagongshe.com/reaction/877193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantIsobutyleneHCID 8255—
Reactant(2S)-Cyclopentyl-(4-methylphenyl)acetic acidHCID 28293121—
SolventDichloromethaneHCID 6344—
Producttert-Butyl(2S)-cyclopentyl-(4-methylphenyl)acetateHCID 54452340—

Reaction Steps

160 g (732.9 mmol) of (2S)-cyclopentyl-(4-methylphenyl)acetic acid were initially charged in 480 ml of dichloromethane, and 2.1 ml of sulfuric acid and 172 ml (1722.4 mmol) of condensed 2-methylprop-1-ene were added at 10° C. The mixture was stirred at RT overnight. If required, the addition of sulfuric acid and 2-methylprop-1-ene was repeated until all the starting material had been consumed. After the reaction had ended, 21 g of potassium carbonate were added and the mixture was stirred for another 2-3 h (evolution of gas). The mixture was then diluted with 700 ml of water and extracted with ethyl acetate. The organic phase was dried over sodium sulfate, filtered and concentrated on a rotary evaporator. The crude product was purified by chromatography on silica gel (mobile phase cyclohexane/ethyl acetate 4:1). This gave 172 g (85% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987256B2
Source datasetuspto-grants-2015_03
ORD IDord-e2b5a3091f3d4d1fbcdb3950a28152c8
Source noteuspto-grants-2015_03