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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059756Generated: November 1, 2026

Isopropanol → Isopropyl 4-methyl-1,2,3-thiadiazole-5-carboxylate

https://huagongshe.com/reaction/1059756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantSodium ChlorideHCID 5234—
ReactantTriethylamineHCID 8471—
Reactant4-Methyl-1,2,3-thiadiazole-5-carboxylic acidHCID 1381992—
CatalystDimethylformamideHCID 6228—
SolventThionyl ChlorideHCID 24386—
ProductIsopropyl 4-methyl-1,2,3-thiadiazole-5-carboxylateHCID 1205638979%

Reaction Steps

To 1.0 g (6.9 mmoles) of 4-methyl-1,2,3-thiadiazole-5-carboxylic acid were added 40 ml of thionyl chloride and 2 drops of dimethylformamide at room temperature, and the resulting mixture was refluxed with heating or 3 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and the excess thionyl chloride was distilled off and 7.0 ml of tetrahydrofuran was added to the residue. Then, 2.1 g (21 mmoles) of triethylamine and 0.83 g (13.8 mmoles) of isopropanol were added and the resulting mixture was stirred at room temperature for 18 hours, after which a saturated aqueous sodium chloride solution was added. The desired compound was extracted with ethyl acetate and the organic layer was washed successively with diluted hydrochloric acid, a saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by a silica gel column chromatography (n-hexane:ethyl acetate=10:1) to obtain 1.0 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521649B1
Source datasetuspto-grants-2003_02
ORD IDord-ceb1b29c447c4ea39a837107449bc646
Source noteuspto-grants-2003_02