2,5-Dichloronitrobenzene → 1-(4-Chloro-2-nitrophenyl)indoline

HRID 4055

Reaction equation

HRID 4055 reaction equation
Cl[C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[NH:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14][CH2:13]1>CN(C)C=O>[Cl:8][C:5]1[CH:6]=[CH:7][C:2]([N:12]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[CH2:14][CH2:13]2)=[C:3]([N+:9]([O-:11])=[O:10])[CH:4]=1

Participants

4

Procedure

A stirred solution of 38.4 g (0.20 mole) of 1,4-dichloro-2-nitrobenzene and 59.6 g (0.50 mole) of indoline in 400 ml of dimethylformamide (DMF) was heated under nitrogen at 140°-145° C. overnight (23 hours). The DMF solvent was then removed in vacuo and the residue was dissolved in 500 ml of dichloromethane. This solution was extracted with H2O, with dilute hydrochloric acid, with brine, then dried over Na2SO4 and concentrated to an oil. This was adsorbed on a tall chromatography column containing 1.5 kg of silica gel packed in toluene. Elution with toluene brought forth 22.1 g (40% overall yield) of product, which crystallized. A small portion was recrystallized from hexane to afford 1-(4-chloro-2-nitrophenyl)indoline, m.p. 97°-99° C.

Workup

  1. customThe DMF solvent was then removed in vacuo
  2. dissolutionthe residue was dissolved in 500 ml of dichloromethane
  3. extractionThis solution was extracted with H2O, with dilute hydrochloric acid, with brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated to an oil
  6. additioncontaining 1.5 kg of silica gel
  7. washElution with toluene
  8. custom22.1 g (40% overall yield) of product, which
  9. customcrystallized
  10. customA small portion was recrystallized from hexane

Sources & evidence

ORD record
ord-a070677bb7a34268aa9e3cb9e14d0546
Source dataset
uspto-grants-1988_02
Patent number
US04723003

Linked notes

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