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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052900Generated: October 30, 2026

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

https://huagongshe.com/reaction/2052900

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-oxo-octyl)-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 HCl (11.0M aqueous) 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 numberUS07326716B2
Source datasetuspto-grants-2008_02
ORD IDord-67fe7773134c41debb65002de76f75bb
Source noteuspto-grants-2008_02