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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650966Generated: October 30, 2026

Benzyl Bromide → HCID 86584312, compound

https://huagongshe.com/reaction/650966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant3-PyridinemethanolHCID 7510—
SolventEthanolHCID 702—
ProductHCID 86584312HCID 86584312—

Reaction Steps

To a solution of 3-pyridyl carbinol (100 mmol) in 30 mL of ethanol is added benzyl bromide (110 mmol) dropwise via addition funnel at room temperature. Stirring is continued for 2 hours at room temperature and solvents are removed in vacuo. The residue is taken up into acetonitrile (100 mL) and washed with hexanes (3×100 mL). The acetonitrile layer is concentrated in vacuo and dried under vacuum to provide N-benzyl-3-pyridyl carbinol bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277865B1
Source datasetuspto-grants-2001_08
ORD IDord-debc630d7a834f53b72f7d4b5c9a69c8
Source noteuspto-grants-2001_08