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

HRID 741551
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HRID 741551 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

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

생성물 1

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

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-a438be55064d4e95826bca58cff609d1
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05552399

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