Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657176Generated: October 29, 2026

Methanol → 3-(Aminomethyl)-1-benzylpiperidin-4-ol

https://huagongshe.com/reaction/657176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
ReactantHCID 68684193HCID 68684193—
SolventTetrahydrofuranHCID 8028—
Product3-(Aminomethyl)-1-benzylpiperidin-4-olHCID 2300373251%

Reaction Steps

A suspension of 4-hydroxy-1-(phenylmethyl)-3-piperidinecarboxamide (5.62 g, 23.9 mmol) in THF (65 mL) was treated dropwise with borane-methyl sulphide complex (2M solution in THF, 26.4 mL, 52.8 mmol). After stirring for 0.5 h at room temperature, the reaction mixture was heated at 80° C. for 1.5 h. Methanol (16 mL) was added and heating continued for 0.5 h. The mixture was evaporated and the residue was chromatographed on silica gel, eluting with 10-30% (2M ammonia/methanol)/dichloromethane to give the product (2.67 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-2a805150c29f4d3598fcd09386911c3a
Source noteuspto-grants-2011_12