HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019067Generated: October 26, 2026
4'-Bromoacetanilide → N-[4-[2-(dimethylamino)-2-methyl-1-oxopropyl]phenyl]acetamide
https://huagongshe.com/reaction/1019067
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4'-Bromoacetanilide | HCID 7683 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-(Dimethylamino)-2-methylpropanenitrile | HCID 10510831 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Product | N-[4-[2-(dimethylamino)-2-methyl-1-oxopropyl]phenyl]acetamide | HCID 22603032 | 36% |
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-di-methylethanamine (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06486187B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-4abf1ff902194525913aa2663fdd2baf |
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| Source note | uspto-grants-2002_11 |
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