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HRID 2061297생성일: 2026년 10월 26일

Butanediol → Butanediol bis(3-mercaptobutyrate)

https://huagongshe.com/reaction/2061297

반응식

참여 물질

역할이름HCID투입량
반응물ButanediolHCID 165788—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물3-Mercaptobutyric acidHCID 9964084—
용매TolueneHCID 1140—
생성물Butanediol bis(3-mercaptobutyrate)HCID 87175182—

반응 조건

온도140 °C

반응 단계

In a 300 ml egg plant type flask, 20 g (222 mmol) of butanediol (available from Wako Pure Chemical Industries, Ltd.), 58.7 g (488 mmol) of 3-mercaptobutanoic acid (available from Yodo Chemical Co., Ltd.), 2.78 g (14.6 mmol) of p-toluenesulfonic acid monohydrate (available from Junsei Chemical Co., Ltd.) and 100 g of toluene (available from Junsei Chemical Co., Ltd.) were placed, and a Dean-Stark device and a cooling tube were installed. The contents in the flask were heated at an oil bath temperature of 140° C. with stirring. After 4 hours from the initiation of reaction, the reaction solution was allowed to cool, washed with ion-exchanged water and then neutralized with a saturated sodium hydrogencarbonate aqueous solution. The resulting solution was further washed with ion-exchanged water three times and then subjected to dehydration-drying using anhydrous magnesium sulfate (available from Junsei Chemical Co., Ltd.). Next, toluene was distilled off, and the remainder was subjected to column chromatography by a silica gel to perform purification of BDMB. As the silica gel, Wako gel C-200 (available from Wako Pure Chemical Industries, Ltd.) was used, and as the elution solvent, n-hexane/acetone (7/1 by volume) was used. The BDMB obtained by purification was a colorless transparent liquid, and the yield was 31.1 g (48%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08283095B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-8d32ae675d6844d19c505da4e0ac1bd0
출처 메모uspto-grants-2012_10