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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096260Generated: November 1, 2026

Sodium borohydride → HCID 66783140, compound

https://huagongshe.com/reaction/1096260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66783161HCID 66783161—
SolventEthanolHCID 702—
ProductHCID 66783140HCID 6678314049.1%

Reaction Steps

Sodium borohydride (59 mg, 1.6 mmol) was added at RT to a solution of 4-(tert-butyl-diphenyl-silanyloxy)-2-[3-methyl-2-oxo-4-(3-trifluoromethyl-phenyl)-piperazin-1-yl]-butyric acid methyl ester (480 mg, 0.78 mmol) in EtOH (7 mL), then after 20 h the reaction mixture was partitioned between 10% aq. KHSO4 solution and CH2Cl2. The organic layer was dried (MgSO4), filtered, and evaporated. Chromatography (SiO2; heptane/EtOAc 4:1) afforded the title compound (224 mg, 49%). Light yellow oil, MS: 585.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138175B2
Source datasetuspto-grants-2012_03
ORD IDord-09722c1f69b84654b022b7903e014c79
Source noteuspto-grants-2012_03