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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453095Generated: October 25, 2026

Sodium borohydride → [3-(4-Methoxyphenyl)-[1,2,4]thiadiazol-5-yl]-methanol

https://huagongshe.com/reaction/453095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 3-(4-methoxyphenyl)-[1,2,4]thiadiazole-5-carboxylateHCID 12601460—
SolventMethanolHCID 887—
Product[3-(4-Methoxyphenyl)-[1,2,4]thiadiazol-5-yl]-methanolHCID 2513288543%

Reaction Steps

To a solution of 3-(4-methoxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester (0.24 g, 0.90 mmol) in MeOH (10 ml) was added sodium borohydride (0.058 g, 1.54 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. The crude residue was purified over silica gel (100-200 M, 20% EtOAc-Hexane) to get the product (0.072 g, 43%) 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-e2b1241a7bfc40cd8521af8989048b08
Source noteuspto-grants-2013_07