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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706647Generated: October 29, 2026

Methyl 6-methylnicotinate → (6-Methylpyridin-3-yl)methanol

https://huagongshe.com/reaction/706647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 6-methylnicotinateHCID 231548—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(6-Methylpyridin-3-yl)methanolHCID 1122878864%

Reaction Steps

A solution of methyl 6-methylnicotinate (16.3 g, 108 mmol) in MeOH (150 mL) was treated with sodium borohydride (12.2 g, 323 mmol) at ambient temperature in portions. The mixture was quenched with water (100 mL) and concentrated. This mixture was diluted with water (300 mL) and extracted with EtOAc. The combined organic extracts were dried (phase separator silicone treated filter paper) and concentrated to give (6-methylpyridin-3-yl)methanol (8.5 g, 64% yield) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174981B2
Source datasetuspto-grants-2015_11
ORD IDord-56f6f8d3f0f84a068123bd9030f0f0e8
Source noteuspto-grants-2015_11