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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559128Generated: October 30, 2026

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

https://huagongshe.com/reaction/559128

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 numberUS08063070B2
Source datasetuspto-grants-2011_11
ORD IDord-f16af00c10c54f8d9ae0226199f22831
Source noteuspto-grants-2011_11