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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263833생성일: 2026년 10월 26일

1-Bromohexadecane → HCID 14350902, 화합물

https://huagongshe.com/reaction/263833

반응식

참여 물질

역할이름HCID투입량
반응물1-BromohexadecaneHCID 8213—
반응물Sodium hydrideHCID 24758—
반응물3-Trityloxypropane-1,2-diolHCID 2882827—
용매DimethylformamideHCID 6228—
생성물HCID 14350902HCID 1435090268.3%

반응 단계

1H-nmr (200 MHz, CDCl3), 3.21 (2H, m), 3.65 (2H, m), 3.85 (1H, m), 7.4 (15H, m). ##STR17## Sodium hydride (prewashed with hexane, 60% oil dispersion, 0.79 g, 32.89 mmol) was stirred in dry dimethyl formamide (50 ml) under a stream of nitrogen. 1-trityl glycerol (5.0 g, 14.95 mmol) in dry dimethyl formamide (50 ml) was added carefully. The reaction was stirred at room temperature for 30 minutes before 1-bromohexadecane (9.13 g, 29.90 mmol) was added and the reaction was stirred at room temperature under a nitrogen atmosphere for 12 hours. The reaction mixture was carefully partitioned between dichloromethane (100 ml) and water (100 ml×3). The organic layer was washed successively with saturated NaHCO3 (100 ml) and brine (100 ml), dried over sodium sulphate and evaporated to yield the crude product, which was purified by column chromatography eluting with (40-60) light petroleum: ethyl acetate (230:20). Fractions containing product were evaporated to dryness to give 1,2-dihexadecyl-3-trityl glycerol (8.00 g, 10.21 mmol) 68% yield

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05645883
출처 데이터셋uspto-grants-1997_07
ORD IDord-01fff633c6774e4eb8c309ed33313eba
출처 메모uspto-grants-1997_07