4-Bromoaniline → 1-(4-Bromophenyl)pyrrolidin-2-one

HRID 1003703Notes

Reaction equation

HRID 1003703 reaction equation
[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl[CH2:17][CH2:18][CH2:19][C:20](Cl)=[O:21].CC(C)([O-])C.[K+]>C1COCC1.C(OCC)(=O)C.C([O-])([O-])=O.[Na+].[Na+].O>[Br:1][C:2]1[CH:8]=[CH:7][C:5]([N:6]2[CH2:17][CH2:18][CH2:19][C:20]2=[O:21])=[CH:4][CH:3]=1

Participants

9

Conditions

Temperature
5 °C

Procedure

To a solution of 4-bromoaniline (10 g, 58 mmol) in dry THF (150 ml), under argon was added triethylamine (6 g, 59 mmol) and 4-chlorobutyryl chloride (8.2 g 58 mmol) at 5° C. The mixture was stirred at 5° C. for 40 mins and potassium tert-butoxide (16 g, 142 mmol) added in one portion. After 10 mins the mixture was warmed to 25° C. and stirred for 4 hours, then left to stand overnight. Water (10 ml) was added and the mixture stirred for 30 mins. The mixture was diluted with ethyl acetate (200 ml) and 3% Na2CO3 (aq) (120 ml). The aqueous layer was reextracted with ethyl acetate (100 ml) and the combined extracts dried over Na2SO4. The solvent was evaporated in vacuo to give a brown solid (12 g). Chromatography on silica gel (~200 g) using 30-60% ethyl acetate/hexane gradient elution gave the tide compound as a yellow crystalline solid (10.24 g, 74%).

Workup

  1. temperatureAfter 10 mins the mixture was warmed to 25° C.
  2. stirringstirred for 4 hours
  3. waitleft
  4. waitto stand overnight
  5. stirringthe mixture stirred for 30 mins
  6. dry with materialthe combined extracts dried over Na2SO4
  7. customThe solvent was evaporated in vacuo

Sources & evidence

ORD record
ord-e53a991a20c34d9ba8a1809a59cdfb58
Source dataset
uspto-grants-2000_04
Patent number
US06046210

Reaction notes

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