Aspirin → HCID 10424739、化合物

HRID 616191ノート

反応式

HRID 616191 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[OH:10].C([O:14][C:15]1[C:16](=[CH:20][CH:21]=[CH:22][CH:23]=1)[C:17](O)=[O:18])(=O)C>CC(C)=O.N1C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[C:6]([CH:5]=[C:4]([Cl:9])[C:3]=1[OH:10])[NH:8][C:17](=[O:18])[C:16]1[CH:20]=[CH:21][CH:22]=[CH:23][C:15]=1[OH:14]

参加物

5

実験手順

2,6-Dichloro-4-aminophenol (0.37 g.) was dissolved in acetone (30 ml.) to which pyridine (0.32 ml.) was added. While mixing, an acetone solution (10 ml.) of the acid chloride prepared from acetylsalicylic acid (0.38 g.) was added by drops. After the reaction was completed, the solution was evaporated under reduced pressure and the residue was dissolved in ethyl acetate and then was washed with water then with 1N-hydrochloric acid. After evaporating off the ethyl acetate under reduced pressure the resulting residue was dissolved in a mixture of methanol and 2N-sodium hydroxide (10 ml. each). The solution was agitated for several hours then acidified with 2N-hydrochloric acid to precipitate the product. By recrystallization in acetone-water, white needle-like crystals of 3',5'-dichloro-2,4'-dihydroxybenzanilide (0.62 g.) were obtained. The yield was 78% and the melting point was 217-219° C.

後処理

  1. additionwas added
  2. additionWhile mixing
  3. additionwas added by drops
  4. customthe solution was evaporated under reduced pressure
  5. dissolutionthe residue was dissolved in ethyl acetate
  6. washwas washed with water
  7. customAfter evaporating off the ethyl acetate under reduced pressure the resulting residue
  8. dissolutionwas dissolved in a mixture of methanol and 2N-sodium hydroxide (10 ml
  9. customto precipitate the product
  10. customBy recrystallization in acetone-water

出典と根拠

ORDレコード
ord-f508a53b631c41d889be6ed10b0b259d
出典データセット
uspto-grants-1978_02
特許番号
US04072753

反応ノート

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