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Hexane → 6-Methoxy-3,4-dihydroisoquinoline

HRID 484391
ノート
印刷プレビュー

反応式

HRID 484391 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 100121966-Methoxy-3,4-dihydroisoquinoline収率 87%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-e0ea5fc509584806bf031f01dfd6b5de
出典データセット
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05231181

反応ノート

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