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

HRID 34312

반응식

HRID 34312 반응식
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

참가 물질

4

반응물 2

HCID 69772,5-DichloronitrobenzeneHCID 10328Indoline

생성물 1

HCID 138233221-(4-Chloro-2-nitrophenyl)indoline

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

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. alignment 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.

후처리

  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

출처 및 근거

ORD 기록
ord-4614d22a5e664483a2a097a756e691f7
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04761411

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