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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5666생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/5666

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Oxalic AcidHCID 971—
반응물DiisobutylaluminumhydrideHCID 21225700—
반응물2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 53657145—
용매TolueneHCID 1140—
용매HexaneHCID 8058—
생성물2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenalHCID 5444191884%

반응 조건

온도-70 °C

반응 단계

To a solution of 2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile (856 mg, 3.0 mmol) in n-hexane (30 ml) was added a 0.5 M solution of diisobutylaluminium hydride in toluene (6 ml) with stirring at -70° C. under argon atmosphere. After one hour, water (3 ml) was added, the cooling bath was removed, and the reaction mixture was stirred well. Resultant white precipitates were filtered and washed. The filtrate was concentrated to give a residue, which was dissolved in n-hexane (10 ml). The n-hexane solution was combined with a 10% aqueous solution of oxalic acid (5 ml) and stirred for 3 hours. The organic layer was extracted and separated, washed with water, dried over MgSO4, and concentrated. The resultant residue was subjected to silica gel column chromatography (solvent: n-hexane/ethyl acetate=10:1) to obtain 2 -(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenal (865 mg, 84%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245085
출처 데이터셋uspto-grants-1993_09
ORD IDord-1beec0472a4d456a82991908e309a084
출처 메모uspto-grants-1993_09