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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224636Generated: October 26, 2026

4'-Bromoacetanilide → N-[4-[2-(dimethylamino)-2-methyl-1-oxopropyl]phenyl]acetamide

https://huagongshe.com/reaction/2224636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-BromoacetanilideHCID 7683—
ReactantTetrahydrofuranHCID 8028—
Reactant2-(Dimethylamino)-2-methylpropanenitrileHCID 10510831—
ReactantCID 53628100HCID 178418400—
ProductN-[4-[2-(dimethylamino)-2-methyl-1-oxopropyl]phenyl]acetamideHCID 2260303236%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Sec butyllithium (298 ml: 1.3 M) was added dropwise at −60° C. under N2 flow to a solution of N-(4-bromophenyl)acetamide (0.1892 mol) in THF (400 ml) and the mixture was stirred at −70° C. for 2 hours. A solution of 1-cyano-1-methyl-N,N-dimethylethanamine (0.075 mol) in THF (60 ml) was added dropwise, the mixture was brought to RT and then stirred at RT for 12 hours. The mixture was poured into ice and extracted with EtOAc. The solvent was evaporated, the residue was taken up in HCl (3 N) and EtOAc, extracted with EtOAc, basified with K2CO3 (10%) and extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was recrystallized from (C2H5)2O and DIPE. The precipitate was filtered off and dried, yielding 6.8 g (36%) of N-[4-[2-(dimethylamino)-2-methyl-1-oxopropyl]phenyl]acetamide (interm. 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378433B2
Source datasetuspto-grants-2008_05
ORD IDord-e84fc058eecb40169ea9f4784068e9d8
Source noteuspto-grants-2008_05