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HRID 263833作成日:2026年10月27日

1-Bromohexadecane → 1,2-Dihexadecyl-3-trityl glycerol

https://huagongshe.com/reaction/263833

反応式

関与物質

役割名称HCID仕込み量
反応物1-BromohexadecaneHCID 8213—
反応物Sodium hydrideHCID 24758—
反応物3-Trityloxypropane-1,2-diolHCID 2882827—
溶媒DimethylformamideHCID 6228—
生成物1,2-Dihexadecyl-3-trityl glycerolHCID 1435090268.3%

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05645883
出典データセットuspto-grants-1997_07
ORD IDord-01fff633c6774e4eb8c309ed33313eba
出典メモuspto-grants-1997_07