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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419942Generated: October 25, 2026

N-Methoxy-N-methylacetamide → 2-(4-Acetylphenyl)-2-methylpropanenitrile

https://huagongshe.com/reaction/419942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methoxy-N-methylacetamideHCID 537505—
Reactant2-(4-Bromophenyl)-2-methylpropanenitrileHCID 10443591—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Acetylphenyl)-2-methylpropanenitrileHCID 5829845779%

Reaction Conditions

Temperature-100 °C

Reaction Steps

2-(4-bromophenyl)-2-methylpropanenitrile (1 g, 4.46 mmol) is dissolved in anhydrous THF (75 ml) the solution is cooled down to −100° C. with a diethyl ether-liquid nitrogen bath, n-butyl lithium 2M in c-hexane (4.0 ml, 8.0 mmol) is added and this reaction mixture stirred for 10 min., then N-methoxy-N-methyl acetamide (1.6 g, 15.6 mmol) is added and the reaction is then left to slowly warm-up to room temperature. After work-up (washing with acidic brine) and concentration the crude mixture is purified on silica gel using a 0 to 50% ethyl acetate in hexane gradient, to give the desired compound (660 mg, 78%) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093402B2
Source datasetuspto-grants-2012_01
ORD IDord-0b06eb5bd69d403db9ed2fc14906cc56
Source noteuspto-grants-2012_01