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Hexane → 6-Methoxy-3,4-dihydroisoquinoline

HRID 484391
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HRID 484391 반응식
[CH:1]([NH:3][CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([O:12][CH3:13])[CH:7]=1)=O.P(Cl)(Cl)(Cl)(Cl)Cl.CCCCCC>ClCCl>[CH3:13][O:12][C:8]1[CH:7]=[C:6]2[C:11](=[CH:10][CH:9]=1)[CH:1]=[N:3][CH2:4][CH2:5]2
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참가 물질

5

반응물 3

HCID 8058HexaneHCID 24819Phosphorus pentachlorideHCID 13562936N-[2-(3-Methoxyphenyl)ethyl]formamide

생성물 1

HCID 100121966-Methoxy-3,4-dihydroisoquinoline수율 87%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 29.4 Kg of N-formyl-3-methoxyphenethylamine in 30 litres of dichloromethane was added over 90 minutes to a well-stirred slurry of 38.4 Kg of phosphorus pentachloride in 30 litres of dichloromethane. An exothermic reaction ensued, causing the solvent to reflux at 35°-38° C. After addition was complete, the reaction mixture was hydrolysed by the addition of a mixture of 90 Kg of ice and 30 litres of hexane. After cooling the aqueous layer was separated, made basic with 144 Kg of 45% potassium hydroxide and extracted twice with 50 Kg of dichloromethane. After drying the organic layer with sodium sulfate the solvent was removed under reduced pressure to give 23 Kg of 6-methoxy-3,4-dihydroisoquinoline as an oil.

후처리

  1. customAn exothermic reaction
  2. temperatureto reflux at 35°-38° C
  3. additionAfter addition
  4. temperatureAfter cooling the aqueous layer
  5. customwas separated
  6. extractionextracted twice with 50 Kg of dichloromethane
  7. dry with materialAfter drying the organic layer with sodium sulfate the solvent
  8. customwas removed under reduced pressure

출처 및 근거

ORD 기록
ord-e0ea5fc509584806bf031f01dfd6b5de
출처 데이터셋
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05231181

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