Hydrochloric Acid → 6,7-dihydro-5H-dibenzo[a,c]-cyclohepten-4-carboxamide

HRID 2412567노트

반응식

HRID 2412567 반응식
[CH:1]1[C:6]2[C:7]3[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=3[CH2:9][CH2:10][CH2:11][C:5]=2[C:4]([C:16]#[N:17])=[CH:3][CH:2]=1.Cl.C([OH:21])C>[OH-].[Na+]>[CH:1]1[C:6]2[C:7]3[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=3[CH2:9][CH2:10][CH2:11][C:5]=2[C:4]([C:16]([NH2:17])=[O:21])=[CH:3][CH:2]=1

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 132813406,7-dihydro-5H-dibenzo[a,c]cyclohepten-4-carbonitrile

생성물 1

HCID 133912786,7-dihydro-5H-dibenzo[a,c]-cyclohepten-4-carboxamide

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

Under a dry nitrogen atmosphere a stirred mixture of 6,7-dihydro-5H-dibenzo[a,c]cyclohepten-4-carbonitrile (1.0 gram, 0.0045 mole) in ethanol (20 ml) and 10% aqueous sodium hydroxide (20 ml) was heated at reflux for two days. The mixture was cooled and poured into dilute hydrochloric acid (150 ml). The resulting mixture was extracted with five 100 ml portions of methylene chloride and the extracts combined. The combined extracts were washed with two 100 ml portions of water, dried over anhydrous magnesium sulfate and filtered. The solvent was removed from the filtrate by distillation under reduced pressure to leave 6,7-dihydro-5H-dibenzo[a,c]cyclohepten-4-carboxamide as a white solid (1.1 grams, mp>250°).

후처리

  1. temperaturewas heated
  2. temperatureat reflux for two days
  3. temperatureThe mixture was cooled
  4. extractionThe resulting mixture was extracted with five 100 ml portions of methylene chloride
  5. washThe combined extracts were washed with two 100 ml portions of water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customThe solvent was removed from the filtrate by distillation under reduced pressure

출처 및 근거

ORD 기록
ord-e790eb2ad45443c69121c62b64a4a8f2
출처 데이터셋
uspto-grants-1985_01
특허 번호
US04493844

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