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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963012Generated: October 29, 2026

Sodium borohydride → HCID 16756661, compound

https://huagongshe.com/reaction/1963012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12351253HCID 12351253—
SolventEthanolHCID 702—
ProductHCID 16756661HCID 1675666174%

Reaction Steps

To a solution of 3-(4-chlorophenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester (0.85 g, 3.16 mmol) in EtOH (30 ml) was added sodium borohydride (0.30 g, 7.90 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 10 ml of water and concentrated under vacuum. Added 100 ml water 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 desired product (0.53 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415383B2
Source datasetuspto-grants-2013_04
ORD IDord-32cea47595a54149b0b7f3e12a6db713
Source noteuspto-grants-2013_04