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Acetic Acid → 5-Chloro-1,2,3,4-tetrahydroquinoline

HRID 1649418
ノート
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反応式

HRID 1649418 の反応式
[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][C:6](=O)[NH:7]2.[BH4-].[Na+].C(O)(=O)C>O1CCOCC1>[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][NH:7]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 176Acetic AcidHCID 4311764Sodium borohydrideHCID 190277365-chloro-3,4-dihydroquinolin-2(1H)-one

生成物 1

HCID 114806665-Chloro-1,2,3,4-tetrahydroquinoline収率 91.8%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

42.5 g of 5-chloro-3,4-dihydrocarbostyril was suspended in 250 ml of dioxane and 44.3 g of NaBH4 was added to the suspension. Then 67 ml of acetic acid (d=1.05) was added dropwise to the mixture at room temperature. After heat-refluxing the resulting mixture for 2 hours the solvent was removed under reduced pressure. Water was added to the residue and insoluble materials were removed by filtration followed by washing with diethyl ether. The residue was extracted with diethyl ether, dried over anhydrous sodium sulfate and distilled under reduced pressure to obtain 36.0 g of 5-chloro-1,2,3,4-tetrahydroquinoline having a boiling point of 116° to 120° C./0.2 mmHg.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureAfter heat-refluxing the resulting mixture for 2 hours the solvent
  2. customwas removed under reduced pressure
  3. additionWater was added to the residue and insoluble materials
  4. customwere removed by filtration
  5. washby washing with diethyl ether
  6. extractionThe residue was extracted with diethyl ether
  7. dry with materialdried over anhydrous sodium sulfate
  8. distillationdistilled under reduced pressure

出典と根拠

ORDレコード
ord-10951722a7e14f76ab94d25cfddc71cb
出典データセット
uspto-grants-1983_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04416884

反応ノート

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