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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453113Generated: October 29, 2026

Sodium borohydride → (3-(4-Chloro-2-methoxyphenyl)-1,2,4-thiadiazol-5-yl)methanol

https://huagongshe.com/reaction/453113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 3-(4-chloro-2-methoxyphenyl)-1,2,4-thiadiazole-5-carboxylateHCID 59549519—
SolventEthanolHCID 702—
Product(3-(4-Chloro-2-methoxyphenyl)-1,2,4-thiadiazol-5-yl)methanolHCID 5954952892%

Reaction Steps

To a solution of ethyl 3-(4-chloro-2-methoxyphenyl)-1,2,4-thiadiazole-5-carboxylate (0.31 g, 1.04 mmol) in EtOH (15 ml) was added sodium borohydride (0.098 g, 2.59 mmol) portion wise. The resulting reaction mixture was stirred at room temperature for 2 h. After the completion of the reaction (TLC monitoring), the reaction mass was cooled to 0° C., quenched it with 2 ml of water and concentrated under vacuum. Added water (50 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layer was dried over Na2SO4, filtered and concentrated under vacuum to get the product (0.22 g, 92%) that was carried forward to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492414B2
Source datasetuspto-grants-2013_07
ORD IDord-1f964dd4b88b4e8582cb768019234da5
Source noteuspto-grants-2013_07