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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919809Generated: November 3, 2026

Sodium borohydride → HCID 57951159, compound

https://huagongshe.com/reaction/1919809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57951114HCID 57951114—
SolventEthanolHCID 702—
ProductHCID 57951159HCID 5795115967%

Reaction Steps

Stir 4-(3-fluoro-phenyl)-N-(4-trifluoromethoxy-phenyl)-4-oxo-butyramide (3.0 g, 8.5 mmol) in ethanol (70 mL) at room temperature. Add sodium borohydride (650 mg, 17.2 mmol) portionwise and stir at room temperature until TLC indicates that no starting material remains. Add acetone to quench excess borohydride, concentrate the reaction mixture under reduced pressure, redissolve in ethyl acetate and wash with brine. Dry over anhydrous magnesium sulfate, evaporate under reduced pressure to give the titled compound (2.0 g, 67% yield) MS (m/z): 358(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168659B2
Source datasetuspto-grants-2012_05
ORD IDord-4e2af5c27e4042378e0bcf888c2fab39
Source noteuspto-grants-2012_05