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Sodium Hydroxide → 4-Chloro-2-{[2-chloro-4-(ethylsulfonyl)phenyl]thio}aniline

HRID 910835
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HRID 910835 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-])=O)=[C:4]([S:11][C:12]2[CH:17]=[CH:16][C:15]([S:18]([CH2:21][CH3:22])(=[O:20])=[O:19])=[CH:14][C:13]=2[Cl:23])[CH:3]=1.[OH-].[Na+]>C(O)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([S:11][C:12]2[CH:17]=[CH:16][C:15]([S:18]([CH2:21][CH3:22])(=[O:20])=[O:19])=[CH:14][C:13]=2[Cl:23])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 673916204-Chloro-2-{[2-chloro-4-(ethylsulfonyl)phenyl]thio}-1-nitrobenzene

생성물 1

HCID 673913764-Chloro-2-{[2-chloro-4-(ethylsulfonyl)phenyl]thio}aniline

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

The product from step (ii) (0.80 g) and reduced iron powder (0.80 g) in glacial acetic acid (30 ml) was vigorously stirred at RT for 2 h. The mixture was filtered through celite, and the filtrate evaporated under reduced pressure to give a brown oil which was neutralised with 2M NaOH and extracted with ethyl acetate. The organics were dried, evaporated under reduced pressure and the residue purified by chromatography on silica eluting with isohexane/ethylacetate 2:1, yield 0.70 g.

후처리

  1. filtrationThe mixture was filtered through celite
  2. customthe filtrate evaporated under reduced pressure
  3. customto give a brown oil which
  4. extractionextracted with ethyl acetate
  5. customThe organics were dried
  6. customevaporated under reduced pressure
  7. customthe residue purified by chromatography on silica eluting with isohexane/ethylacetate 2:1, yield 0.70 g

출처 및 근거

ORD 기록
ord-6a7813e3f86c462a816d715d542eae55
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022248B2

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