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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 888749생성일: 2026년 10월 24일

Methyl 3-oxoicosanoate → Icosane-1,3-diol

https://huagongshe.com/ko/reaction/888749

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-oxoicosanoateHCID 84502—
반응물Lithium borohydrideHCID 4148881—
용매TetrahydrofuranHCID 8028—
생성물Icosane-1,3-diolHCID 25229601—

반응 단계

Methyl 3-oxoicosanoate (5.2 g, 15.3 mmoles) is dissolved in anhydrous tetrahydrofuran (31 mL) and this solution is added slowly dropwise to an ice-cooled solution of lithium borohydride in anhydrous tetrahydrofuran (2 M, 31 mL, 61.2 mmoles). When the addition is complete, the cooling bath is removed and the reaction is stirred at ambient temperature for 16 hours. The clear, colorless solution is again cooled in an ice bath, and aqueous hydrochloric acid (1 M, 62 mL) is added slowly dropwise to decompose the excess reducing agent (gas is evolved). When a homogeneous solution is obtained, the mixture is concentrated to remove tetrahydrofuran. Methylene chloride (100 mL) is added; the mixture is shaken well and poured into a separatory funnel. The layers are allowed to separate and the bottom aqueous layer is drawn off. The aqueous layer is then washed once more with methylene chloride (100 mL), and the combined methylene chloride solutions are washed with saturated aqueous sodium chloride (50 mL). The methylene chloride solution is then dried over anhydrous sodium sulfate, filtered and co-evaporated five times with methanol (50 mL each) to dryness. The oil is dried well in vacuo. The yield is 3.7 g (77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08252755B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-efd20c1157f343b281bbed0212196600
출처 메모uspto-grants-2012_08