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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505298Generated: November 1, 2026

Sodium borohydride → HCID 178471787, compound

https://huagongshe.com/reaction/505298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178471786HCID 178471786—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178471787HCID 178471787—

Reaction Steps

Sodium borohydride (62.3 mg, 1.65 mmol) was added to a stirred solution of ethyl (trans-4-{[ethyl(2-formylpyridin-3-yl)amino]methyl}cyclohexyl)acetate (136.9 mg, 0.412 mmol) in EtOH (10 mL) at room temperature. The reaction was stirred at room temperature for 1 h, then diluted with water and most of the EtOH was removed in vacuo. The resulting aqueous slurry was extracted with EtOAc (3×20 mL) and the combined extracts were washed with brine (5 mL), dried (Na2SO4) and concentrated in vacuo to afford ethyl [trans-4-({ethyl[2-(hydroxymethyl)pyridin-3-yl]amino}methyl)cyclohexyl]acetate. LCMS calc.=335.2; found=335.3 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781426B2
Source datasetuspto-grants-2010_08
ORD IDord-1147798b5241454c8c71794e552293a8
Source noteuspto-grants-2010_08