돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238172생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/238172

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-BromobutaneHCID 6554—
반응물tert-Butyl (4-methylphenyl)acetateHCID 12362014—
반응물Potassium tert-butoxideHCID 23665647—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 3-methyl-2-(4-methylphenyl)pentanoateHCID 58074556—

반응 조건

온도0 °C

반응 단계

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 drowise, and the solution was stirred at 0° C. for 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642592B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-d849c72962184e80be70b139d94a6ff1
출처 메모uspto-grants-2014_02