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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | (2S)-Cyclopentyl-(4-methylphenyl)acetic acid | HCID 28293121 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl(2S)-cyclopentyl-(4-methylphenyl)acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987256B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-e2b5a3091f3d4d1fbcdb3950a28152c8 |
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| Source note | uspto-grants-2015_03 |
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