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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770910Generated: October 31, 2026

Methanol → 3-Bromo-5-(methoxymethyl)benzonitrile

https://huagongshe.com/reaction/1770910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-5-(bromomethyl)benzonitrileHCID 14567861—
SolventDimethylformamideHCID 6228—
Product3-Bromo-5-(methoxymethyl)benzonitrileHCID 67979398—

Reaction Steps

MeOH (0.088 mL, 2.18 mmol) was added to a slurry of NaH (45 mg, 1.13 mmol) in DMF (2 mL). When gas evolution ceased, a solution of 3-bromo-5-(bromomethyl)benzonitrile (see WO2009/100169; 240 mg, 0.87 mmol) in DMF (1 mL) was added. The reaction was quenched by adding aq. sat NH4Cl solution. The mixture was partitioned between toluene (5 mL) and water (3 mL). The toluene layer was collected, washed with water, dried over Na2SO4, and concentrated in vacuo. The crude product was dried at reduced pressure and used in the next step: GCMS (CI) m/z 226 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248129B2
Source datasetuspto-grants-2016_02
ORD IDord-c96c2b2c52bc47689ab6869f2c083dc8
Source noteuspto-grants-2016_02