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Sulfuric Acid → 9Chloro-6,11-dihydro-5H-dibenz[b,e]azepine

HRID 741551
ノート
印刷プレビュー

反応式

HRID 741551 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][NH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[CH2:16]O)=[CH:4][CH:3]=1.S(=O)(=O)(O)O.[OH-].[K+]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]2[CH2:8][NH:9][C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[CH2:16][C:4]=2[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 1118Sulfuric AcidHCID 14797Potassium HydroxideHCID 14260872(2-{[(4-Chlorophenyl)methyl]amino}phenyl)methanol

生成物 1

HCID 541749289Chloro-6,11-dihydro-5H-dibenz[b,e]azepine収率 95%

実験手順

2-[[(4-chlorophenyl)methyl]amino]benzenemethanol (6.7 g) (prepared as described in J. Chem. Soc. Chem. Commun., 1989 (1), 44-5) was cooled under a N2 atmosphere to -40° C. Sulfuric acid (35 ml) was added dropwise keeping the temperature at about -10° C. and the mixture was stirred at room temperature for 1 hour. The mixture was poured into ice water and basified carefully with KOH. The mixture was filtered off and the precipitate was washed with water and CH2Cl2. The filtrate and the washings were extracted, dried with Na2SO4, filtered off and evaporated, yielding 5.8 g (95%) of 9-chloro-6,11-dihydro-5H-dibenz-[b,e]azepine (interm. 27).

後処理

  1. customat about -10° C.
  2. filtrationThe mixture was filtered off
  3. washthe precipitate was washed with water and CH2Cl2
  4. extractionThe filtrate and the washings were extracted
  5. dry with materialdried with Na2SO4
  6. filtrationfiltered off
  7. customevaporated

出典と根拠

ORDレコード
ord-a438be55064d4e95826bca58cff609d1
出典データセット
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05552399

反応ノート

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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