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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877148Generated: October 26, 2026

Water → Tert-butyl 3-methyl-2-(4-methylphenyl)pentanoate

https://huagongshe.com/reaction/877148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-BromobutaneHCID 6554—
Reactanttert-Butyl (4-methylphenyl)acetateHCID 12362014—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 3-methyl-2-(4-methylphenyl)pentanoateHCID 58074556—

Reaction Conditions

Temperature0 °C

Reaction Steps

Under argon, 19.58 g (174.5 mmol) of potassium tert-butoxide were initially charged in 200 ml of DMF, the mixture was cooled to 0° C., 30 g (145.4 mmol) of tert-butyl(4-methylphenyl)acetate, dissolved in 50 ml of DMF, were added slowly and the mixture was then stirred at 0° C. for 30 min. 18.95 ml (174.5 mmol) of 2-bromobutane were then slowly added dropwise, and the solution was stirred at 0° C. for another 4 h. 200 ml of water and 200 ml of diethyl ether were then added to the reaction solution. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were dried over magnesium sulfate. After filtration, the solvent was removed under reduced pressure. The crude product was purified chromatographically on silica gel (mobile phase cyclohexane/ethyl acetate 20:1). This gave 15.5 g (59.1 mmol, 40.6% of theory) of a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987256B2
Source datasetuspto-grants-2015_03
ORD IDord-2027e2cb67414569a0d57c6e240f03f0
Source noteuspto-grants-2015_03