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HRID 36137생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/36137

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물DimethylformamideHCID 6228—
반응물3-Methyl-1-pentanolHCID 11508—
반응물Sodium hydrideHCID 24758—
반응물Hypobromous acidHCID 83547—
용매MethanolHCID 887—
생성물8-(3-Methylpentyloxy)octanolHCID 22407999—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05412137
출처 데이터셋uspto-grants-1995_05
ORD IDord-4365ea31456546e198c66696939c2a4c
출처 메모uspto-grants-1995_05