돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1391997생성일: 2026년 10월 25일

Trimethylolpropane → Trimethylolpropane tris(3-mercaptobutyrate)

https://huagongshe.com/reaction/1391997

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylolpropaneHCID 6510—
반응물Sodium BicarbonateHCID 516892—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물3-Mercaptobutyric acidHCID 9964084—
용매TolueneHCID 1140—
생성물Trimethylolpropane tris(3-mercaptobutyrate)HCID 86599594—

반응 조건

온도145 °C

반응 단계

In a 100-ml eggplant-shaped flask were charged 2.68 g (20 mmol) of trimethylolpropane (manufactured by Tokyo Kasei Kogyo Co., Ltd.), 7.57 g (63 mmol) of 3-mercaptobutanoic acid, 0.23 g (1.2 mmol) of p-toluenesulfonic acid monohydrate, and 20 g of toluene, and a Dean-Stark apparatus and a condenser tube were equipped thereto. While the contents being stirred, they were heated at an oil bath temperature of 145° C. After 3 hours from the start of the reaction, the reaction mixture was left to cool and neutralized with 50 ml of an aqueous 5% sodium hydrogen carbonate solution. Further, the reaction mixture was washed with deionized water two times, and then dehydrated and dried over anhydrous magnesium sulfate. Then, the toluene was distilled off and the residue was subjected to column chromatography with silica gel to purify TPMB. The silica gel used was Wako Gel C-200, and n-hexane/ethyl acetate=5/1 (by volume ratio) was used as an elution solvent. The TPMB obtained by the purification was a colorless transparent liquid and the yield was 5.63 g (64%). The TPMB had a compositional formula of C18H32O6S3 and a molecular weight of 440.64.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07341828B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-c87d892e05cb4bebb87b5e2c2ca2df3b
출처 메모uspto-grants-2008_03