Hydrochloric Acid → 4-Hydrazinophenyl propionamide hydrochloride

HRID 400183노트

반응식

HRID 400183 반응식
[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]

참가 물질

5

반응물 3

HCID 313Hydrochloric Acid2회HCID 128052284-Aminophenyl propionamideHCID 23668193Sodium Nitrite

생성물 1

HCID 189442744-Hydrazinophenyl propionamide hydrochloride

시약·촉매·용매 1

HCID 962Water용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-215307264b5042f9ac2cce6380c6a6da
출처 데이터셋
uspto-grants-1998_10
특허 번호
US05827871

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