Hydrochloric Acid → 4-Hydrazinophenyl propionamide hydrochloride

HRID 1683258ノート

反応式

HRID 1683258 の反応式
[ClH:1].[NH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH3:13])[C:10]([NH2:12])=[O:11])=[CH:5][CH:4]=1.[N:14]([O-])=O.[Na+]>O>[ClH:1].[NH:2]([C:3]1[CH:4]=[CH:5][C:6]([CH:9]([CH3:13])[C:10]([NH2:12])=[O:11])=[CH:7][CH:8]=1)[NH2:14]

参加物

5

反応物 3

HCID 313Hydrochloric Acid2 回HCID 128052284-Aminophenyl propionamideHCID 23668193Sodium Nitrite

生成物 1

HCID 189442744-Hydrazinophenyl propionamide hydrochloride

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Concentrated hydrochloric acid (4 ml) was added slowly, with cooling and stirring to 4-aminophenyl propionamide (0.80 g), maintaining the temperature below 5° C. To this slurry was added a solution of sodium nitrite (0.37 g) in water (2 ml), dropwise over 15 min, followed by stirring for a further 15 min. The turbid solution thus formed was added portionwise to a cooled, stirred solution of stannous chloride (2.19 g) in conclusion. HCl (4 ml), and the resulting mixture was stirred for 1 h. After filtering, the solution was reduced in volume until an inorganic precipitate formed. This was filtered off, and the filtrate was evaporated to dryness. The residual gum was crystallized from acetic acid to give crude 4-hydrazinophenyl propionamide hydrochloride (1.05 g).

後処理

  1. temperaturewith cooling
  2. temperaturemaintaining the temperature below 5° C
  3. customThe turbid solution thus formed
  4. additionwas added portionwise to a cooled
  5. filtrationAfter filtering
  6. customformed
  7. filtrationThis was filtered off
  8. customthe filtrate was evaporated to dryness
  9. customThe residual gum was crystallized from acetic acid

出典と根拠

ORDレコード
ord-8ee988cc107e4ea38bc2182aadf6cbf9
出典データセット
uspto-grants-1997_06
特許番号
US05637611

反応ノート

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