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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1110174생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1110174

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 0.5M 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 번호US05324869
출처 데이터셋uspto-grants-1994_06
ORD IDord-44f3e5b21991411fa403ac7f1b688cf9
출처 메모uspto-grants-1994_06