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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028977Generated: October 26, 2026

Water → (2-Bromo-3-methylphenyl)(pyrimidin-4-yl)methanol

https://huagongshe.com/reaction/1028977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(2-Bromo-3-methylphenyl)(2-(methylthio)pyrimidin-4-yl)methanoneHCID 67325293—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product(2-Bromo-3-methylphenyl)(pyrimidin-4-yl)methanolHCID 67324212—

Reaction Steps

To a solution of (2-bromo-3-methylphenyl)(2-(methylthio)pyrimidin-4-yl)methanone (0.10 g, 0.309 mmol) in EtOH (10 mL) was added Raney 2800 nickel, slurry, in water (0.022 mL, 3.41 mmol) and the resulting mixture was reflux until starting material was consumed (2 h). The mixture was brought to RT and decanted. The remaining Ni was extracted with DCM/NH3 (2M in MeOH). The combined organic layers were concentrated and the residue obtained was extracted with DCM and the extracts were combined and concentrated to afford a yellow oil as (2-bromo-3-methylphenyl)(pyrimidin-4-yl)methanol which was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-fa29cff280524d65a83d6afcfc645056
Source noteuspto-grants-2014_05