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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965064Generated: October 30, 2026

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

https://huagongshe.com/reaction/1965064

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 numberUS08415483B2
Source datasetuspto-grants-2013_04
ORD IDord-321f846e955640749df791f13e5f839e
Source noteuspto-grants-2013_04