Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534590Generated: October 30, 2026

Sodium borohydride → (1-Methyl-4-piperidinyl)[3-(2-phenylethyl)-2-pyridinyl]methanol

https://huagongshe.com/reaction/1534590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(1-Methylpiperidin-4-yl)[3-(2-phenylethyl)pyridin-2-yl]methanoneHCID 14885588—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(1-Methyl-4-piperidinyl)[3-(2-phenylethyl)-2-pyridinyl]methanolHCID 1991840587.5%

Reaction Steps

To a mixture of 5.0g (16.2 mmole) of (1-methyl-4-piperidinyl)[3-(2-phenylethyl)-2-pyridinyl]methanone (which can be prepared in the same manner as described in Preparative Example 1, Steps A-D) in 70 mL of methanol was added portionwise 0.8 g (21.1 mmole) of sodium borohydride. The next day the solution was concentrated in vacuo to give a slurry which was dissolved in water and extracted with CHCl3. The combined organic portions were dried over MgSO4, filtered, and concentrated in vacuo to provide a liquid which was distilled (bp 190°-195° C. 1 mm Hg) to give 4.4 gms of the title compound as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089496
Source datasetuspto-grants-1992_02
ORD IDord-69f3cc63764c42e49440483911fdb1da
Source noteuspto-grants-1992_02