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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358473Generated: October 25, 2026

Hydrochloric Acid → (2-Dimethylaminomethyl-thiazol-4-yl)-methanol hydrochloride

https://huagongshe.com/reaction/358473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
ReactantEthyl 2-((dimethylamino)methyl)thiazole-4-carboxylateHCID 2039211—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Product(2-Dimethylaminomethyl-thiazol-4-yl)-methanol hydrochlorideHCID 13121938—

Reaction Steps

Alternatively, a mixture of 2.14 g of ethyl 2-dimethylaminomethyl-4-thiazolecarboxylate and 0.38 g of sodium borohydride in 20 ml. of isopropanol was heated with stirring at reflux temperature for about 14 hours. The reaction mixture was cooled, and 2 ml. of water were added carefully followed by 4 ml. of 5N aqueous hydrochloric acid. The volatile constituents were removed by evaporation. Methanol (10 ml.) was added and the mixture heated to refluxing temperature for about one hour. Methanol was removed by evaporation and the residual solids digested in 10 ml. of isopropanol on the steam bath. The isopropanol solution was separated by decantation and the solids reextracted with 10 m. of isopropanol. The isopropanol solutions and extracts were combined and the combined solution filtered while hot to remove insoluble material. The filtrate was chilled and a crystalline solid appeared which separated and was recovered by filtration. Recrystallization of the filter cake from isopropanol gave 1.73 g of 2-dimethylaminomethyl-4-thiazolemethanol hydrochloride melting at 153°-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04468399
Source datasetuspto-grants-1984_08
ORD IDord-52dc833f21ec475daa27250ab564d894
Source noteuspto-grants-1984_08