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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253115Generated: October 25, 2026

Tetrahydrofuran → 4-Acetylthiomethyl-1,2,3-thiadiazole

https://huagongshe.com/reaction/1253115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium thiophen-2-acetateHCID 23678825—
Reactant1,2,3-Thiadiazol-4-ylmethanol methanesulfonateHCID 53789945—
SolventDiethyl EtherHCID 3283—
Product4-Acetylthiomethyl-1,2,3-thiadiazoleHCID 14370535—

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of 1,2,3-thiadiazol-4-ylmethanol methanesulfonate (0.90 g, 4.6 mmol) in tetrahydrofuran (9 mL) was added an aqueous solution (2 mL) of sodium thiolacetate [prepared from thiolacetic acid (0.38 mL, 5.3 mmol) and sodium bicarbonate (0.445 g, 5.3 mmol)]. The resulting mixture was stirred at 23° C. for 1 h and diluted with ether (75 mL). The organic solution was washed with water (3×3 mL), dried (MgSO4) and concentrated. The crude mixture was purified by chromatography (silica gel column: 1.4×19 cm) with 50% ether in hexane as eluting solvent to give 0.60 g (75%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04746736
Source datasetuspto-grants-1988_05
ORD IDord-c15658dc0d6640a38043aece635bc8ab
Source noteuspto-grants-1988_05