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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391997Generated: October 27, 2026

Trimethylolpropane → Trimethylolpropane tris(3-mercaptobutyrate)

https://huagongshe.com/reaction/1391997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylolpropaneHCID 6510—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-Mercaptobutyric acidHCID 9964084—
SolventTolueneHCID 1140—
ProductTrimethylolpropane tris(3-mercaptobutyrate)HCID 86599594—

Reaction Conditions

Temperature145 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07341828B2
Source datasetuspto-grants-2008_03
ORD IDord-c87d892e05cb4bebb87b5e2c2ca2df3b
Source noteuspto-grants-2008_03