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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474233Generated: November 1, 2026

2-(Methyloxy)-4-(2-oxoethyl)benzonitrile → 4-(2-Hydroxypropyl)-2-methoxybenzonitrile

https://huagongshe.com/reaction/1474233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methyloxy)-4-(2-oxoethyl)benzonitrileHCID 77231259—
ReactantHCID 178418573HCID 178418573—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Hydroxypropyl)-2-methoxybenzonitrileHCID 66643878—

Reaction Steps

To a stirred solution of 2-methoxy-4-(2-oxoethyl)benzonitrile (1.5 g, 8.5 mmol) in dichloromethane (30 mL) at 0° C. was added 2.8 mL (8.5 mmol) of a 3.0 M solution of methylmagnesium bromide in THF. The reaction mixture was allowed to warm up to rt and stirred for 12 h. The reaction was then quenched by the addition of 10 mL of 1 N hydrochloric acid and extracted with dichloromethane (2×30 mL). The combined organic extracts were dried with magnesium sulfate, filtered, and concentrated in vacuo. The crude residue was purified on silica (30% EtOAc/hexanes as eluent) to afford 4-(2-hydroxypropyl)-2-methoxybenzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-8ba945e2dd9549b0867eba3ed5c753d0
Source noteuspto-grants-2015_04