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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271315Generated: October 27, 2026

4'-Bromoacetanilide → 4-[2-(Dimethylamino)-2-methyl-1-oxopropyl]phenylacetamide

https://huagongshe.com/reaction/1271315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-BromoacetanilideHCID 7683—
ReactantTetrahydrofuranHCID 8028—
Reactant2-(Dimethylamino)-2-methylpropanenitrileHCID 10510831—
ReactantCID 53628100HCID 178418400—
Product4-[2-(Dimethylamino)-2-methyl-1-oxopropyl]phenylacetamideHCID 131726333—

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]phenylacetamide (interm. 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205312B2
Source datasetuspto-grants-2007_04
ORD IDord-df9edc60734b4f2b86f45cf3aa912375
Source noteuspto-grants-2007_04