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HRID 36137作成日:2026年10月25日

p-Toluenesulfonic acid → 8-(3-Methylpentyloxy)octanol

https://huagongshe.com/reaction/36137

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物DimethylformamideHCID 6228—
反応物3-Methyl-1-pentanolHCID 11508—
反応物Sodium hydrideHCID 24758—
反応物Hypobromous acidHCID 83547—
溶媒MethanolHCID 887—
生成物8-(3-Methylpentyloxy)octanolHCID 22407999—

反応手順

To a solution of 1.67 gms of 3-methyl pentanol in 40 ml of dimethylformamide, 0.62 gms of sodium hydride are added; and the reaction mixture is stirred at room temperature for 1 hour. To this solution is added 4.0 gms of the protected bromo-alcohol and the reaction mixture is stirred at room temperature for 17 hours. The reaction mixture is then partitioned between ethyl acetate and water. The organic layer is washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to give a yellow liquid. To a solution of 4.0 gms of this liquid in 240 ml of methanol is added 0.40 gms of p-toluenesulfonic acid and the reaction is stirred at room temperature for 16 hours. The methanol is removed under reduced pressure, and the residue is partitioned between ethyl acetate and water. The organic layer is washed with aqueous NaHCO3 and brine, then dried over Na2SO4, filtered, and concentrated under vacuum to give 8-(3-methylpentyloxy)octanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05412137
出典データセットuspto-grants-1995_05
ORD IDord-4365ea31456546e198c66696939c2a4c
出典メモuspto-grants-1995_05