Hydrochloric Acid → 4-[(6-Chloropyridazin-3-yl)oxy]aniline

HRID 67158

反応式

HRID 67158 の反応式
[H-].[Na+].[NH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[C:6](Cl)[CH:5]=1.[Cl:12][C:13]1[N:14]=[N:15][C:16](Cl)=[CH:17][CH:18]=1.Cl>CS(C)=O>[Cl:12][C:13]1[N:14]=[N:15][C:16]([O:10][C:7]2[CH:8]=[CH:9][C:4]([NH2:3])=[CH:5][CH:6]=2)=[CH:17][CH:18]=1

参加物

6

実験手順

12 g of sodium hydride was added in portions to a stirred solution of 71.8 g of 1A and 25 g of 3,6-dichloropyridazine in 300 ml of dimethyl sulfoxide, the temperature of the mixture being held at 50° C. The mixture then was stirred for one hour and poured into ice water. The mixture was slightly acidified with dilute hydrochloric acid, and was extracted with methylene chloride. The extract was washed with water, dried (magnesium sulfate) and the solvent was evaporated to give 4-(6-chloro-3-pyridazinyloxy)benzeneamine (1B), as a tan solid, mp: 126°-129° C.

後処理

  1. custombeing held at 50° C
  2. extractionwas extracted with methylene chloride
  3. washThe extract was washed with water
  4. dry with materialdried (magnesium sulfate)
  5. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-3c0a74c576584da0a7ede398eec0b46b
出典データセット
uspto-grants-1982_08
特許番号
US04345076

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