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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264643Generated: October 29, 2026

Water → (1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)methanol

https://huagongshe.com/reaction/1264643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22708810HCID 22708810—
SolventMethanolHCID 887—
Product(1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)methanolHCID 1126415687.6%

Reaction Conditions

Temperature-20 °C

Reaction Steps

1-(Phenylmethyl)4-(hydroxymethyl)-pyridinyl chloride(0.87 mol) was dissolved in methanol (2200 ml) and cooled to −20° C. Sodium borohydride (1.75 mol) was added portionwise under a nitrogen atmosphere. The reaction mixture was stirred for 30 minutes and water (200 ml) was added dropwise. The reaction mixture was partially evaporated, water was added and the reaction mixture was extracted with DCM. The organic layer was separated, dried, filtered and evaporated. The residue was purified over silica gel (eluent: DCM), yielding 155 g of 1,2,3,6-tetrahydro-1-(phenylmethyl)4-pyridinemethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544997B1
Source datasetuspto-grants-2003_04
ORD IDord-73334193d9d84a0d8708a39fcc3cd3ce
Source noteuspto-grants-2003_04