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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453096Generated: October 29, 2026

Sodium borohydride → HCID 16756658, compound

https://huagongshe.com/reaction/453096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 16756983HCID 16756983—
SolventMethanolHCID 887—
ProductHCID 16756658HCID 16756658103.4%

Reaction Steps

To a solution of 3-(4-trifluoromethoxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester (0.11 g, 0.35 mmol) in MeOH (10 ml) was added sodium borohydride (0.022 g, 0.59 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 (0.10 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-8a2786988f884eac8823b1a46ed33357
Source noteuspto-grants-2013_07