Benzene → 2-(S)-amino-3-methyl-1-phenyl-1-pentanone hydrochloride

HRID 2120146노트

반응식

HRID 2120146 반응식
P(Cl)(Cl)(Cl)(Cl)[Cl:2].[NH2:7][C@H:8]([C:13]([OH:15])=O)[C@H:9]([CH2:11][CH3:12])[CH3:10].[Cl-].[Al+3].[Cl-].[Cl-].Cl.[CH:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[ClH:2].[NH2:7][C@@H:8]([CH:9]([CH3:10])[CH2:11][CH3:12])[C:13]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:15]

참가 물질

6

실험 절차

To a stirred suspension of phosphorus pentachloride (31.4 g, 0.151 mmol.) in anhydrous benzene (300 mL) was added L-isoleucine (19.67 g, 0.151 mmol.) under chilling with ice. The mixture was then stirred for 2 hours under chilling with ice, and further stirred for 17 hours at room temperature. The reaction mixture was chilled with ice and anhydrous aluminum chloride (60 g) was portionwise added. The mixture was then slowly heated ed to reflux temperature for a period of 2 hours. The mixture was refluxed for 3 hours, and then chilled with ice. The chilled reaction mixture was slowly added to a mixture of concentrated hydrochloric acid (45 mL) and ice (0-3 kg). The resulting mixture was stirred at 5° C. for 40 min, The precipitated crystals were collected by filtration and washed with benzene. The washed crystals were dried in air to give 2-(S)-amino-3-methyl-1-phenyl-1-pentanone hydrochloride as a white crystalline product (29.2 g, yield! 85%).

후처리

  1. temperatureunder chilling with ice
  2. temperatureunder chilling with ice
  3. stirringfurther stirred for 17 hours at room temperature
  4. additionwas portionwise added
  5. temperatureThe mixture was then slowly heated
  6. temperatureto reflux temperature for a period of 2 hours
  7. temperatureThe mixture was refluxed for 3 hours
  8. temperaturechilled with ice
  9. customThe chilled reaction mixture
  10. stirringThe resulting mixture was stirred at 5° C. for 40 min
  11. filtrationThe precipitated crystals were collected by filtration
  12. washwashed with benzene
  13. customThe washed crystals were dried in air

출처 및 근거

ORD 기록
ord-f30992ba9490470887c2426f38969aad
출처 데이터셋
uspto-grants-2004_02
특허 번호
US06689785B2

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