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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352408Generated: October 30, 2026

Sodium borohydride → 7-[2-(3-Hydroxy-octyl)-6-oxo-piperidin-1-yl]-heptanoic acid methyl ester

https://huagongshe.com/reaction/352408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant7-[2-Oxo-6-(3-oxooctyl)-piperidin-1-yl]-heptanoic acid methyl esterHCID 10021899—
CatalystMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product7-[2-(3-Hydroxy-octyl)-6-oxo-piperidin-1-yl]-heptanoic acid methyl esterHCID 1004461361%

Reaction Steps

Sodium borohydride (24 mg, 0.63 mmol), followed by MeOH (2 drops), was added to a solution of 7-[2-oxo-6-(3-oxooctyl)-piperidin-1-yl]-heptanoic acid methyl ester (23 mg, 0.063 mmol) in CH2Cl2 (1.0 ML) at 0° C. The mixture was allowed to warm to rt. After 4 h at rt, the reaction was quenched with aqueous HCl (1.0 M) and extracted with EtOAc (3×10 mL). The combined organic phase was washed with saturated aqueous NaHCO3 (15 mL) and brine (15 mL) then dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2×3% MeOH/CH2Cl2, gradient) afforded 14 mg (61%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747037B1
Source datasetuspto-grants-2004_06
ORD IDord-22ab9dab4b384eb281587ed8d601a90d
Source noteuspto-grants-2004_06