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5-Chloroquinoline → 5-Chloro-1,2,3,4-tetrahydroquinoline

HRID 1725355
ノート
印刷プレビュー

反応式

HRID 1725355 の反応式
[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2>C(O)(=O)C.C(OCC)C.[Pt]=O>[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 1

HCID 694585-Chloroquinoline

生成物 1

HCID 114806665-Chloro-1,2,3,4-tetrahydroquinoline収率 69%

試薬・触媒・溶媒 3

HCID 82844Platinum oxide (PtO)触媒HCID 176Acetic Acid溶媒HCID 3283Diethyl Ether溶媒

実験手順

A mixture of 5-chloroquinoline (10.0 g) and platinum oxide (50 mg) in acetic acid was shaken under a hydrogen atmosphere at room temperature for 4 hours. The mixture was diluted with diethyl ether and filtered through Celite. The volatiles were removed under reduced pressure and the residue was partitioned between saturated aqueous sodium bicarbonate and ethyl acetate (3×300 mL). The organic extracts were dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified over silica gel and the fractions containing product were combined and concentrated under reduced pressure to provide 7.0 g (69%) of the desired compound.

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. filtrationfiltered through Celite
  2. customThe volatiles were removed under reduced pressure
  3. customthe residue was partitioned between saturated aqueous sodium bicarbonate and ethyl acetate (3×300 mL)
  4. dry with materialThe organic extracts were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified over silica gel
  8. additionthe fractions containing product
  9. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-536e713fbd0b4bc6b54136ff788d108f
出典データセット
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07491716B2

反応ノート

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