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HRID 1391997作成日:2026年10月25日

Trimethylolpropane → Trimethylolpropane tris(3-mercaptobutyrate)

https://huagongshe.com/reaction/1391997

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylolpropaneHCID 6510—
反応物Sodium BicarbonateHCID 516892—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物3-Mercaptobutyric acidHCID 9964084—
溶媒TolueneHCID 1140—
生成物Trimethylolpropane tris(3-mercaptobutyrate)HCID 86599594—

反応条件

温度145 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07341828B2
出典データセットuspto-grants-2008_03
ORD IDord-c87d892e05cb4bebb87b5e2c2ca2df3b
出典メモuspto-grants-2008_03