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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453094Generated: October 29, 2026

Sodium borohydride → HCID 16756661, compound

https://huagongshe.com/reaction/453094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12351253HCID 12351253—
SolventMethanolHCID 887—
ProductHCID 16756661HCID 16756661101.3%

Reaction Steps

To a solution of 3-(4-chlorophenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester (0.20 g, 0.74 mmol) in MeOH (10 ml) was added sodium borohydride (0.048 g, 1.26 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 (0.17 g) 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-a88b10e22d734b4db81bc5fdf7bdad68
Source noteuspto-grants-2013_07