돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5665생성일: 2026년 10월 24일

Water → 2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile

https://huagongshe.com/ko/reaction/5665

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물a FarnesolHCID 3327—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물Phosphonic acid, (1-cyano-2-methylpropyl)-, diethyl esterHCID 11031342—
용매TolueneHCID 1140—
생성물2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 5365714596%

반응 조건

온도-70 °C

반응 단계

To a solution of 2-(diethylphosphono)isovaleronitrile (8.72 g, 40 mmol) in toluene (75 ml) was gradually added a 0.5 M solution of potassium bis(trimethylsilyl)amide in toluene (75 ml) with stirring at -70° C. under argon atmosphere. The cooling bath was removed, and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was cooled to -70° C. again, and farnesol (5.88 g, 26.7 mmol) was added thereto with stirring, and the mixture was allowed to warm to room temperature. After addition of water, the organic layer was separated, washed with saturated aqueous sodium bicarbonate and then saturated aqueous sodium chloride, and dried over MgSO4. The organic layer was separated from MgSO4 by filtration and concentrated to give a residue, which was purified with silica gel column chromatography (solvent: n-hexane/ethyl acetate=100:1) to obtain the aimed 2 -(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile (7.23 g, 96%; 2Z:2E=25.6:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245085
출처 데이터셋uspto-grants-1993_09
ORD IDord-d891efc28e36422aa4bc843ada73ddc3
출처 메모uspto-grants-1993_09