Benzoic acid, 2-hydrazinyl-, hydrochloride (1:1) → 3-(Dimethylamino)-8-carboxy-1,2,3,4-tetrahydrocarbazole

HRID 427145

反応式

HRID 427145 の反応式
CN(C)C1CCC(=O)CC1.Cl.C(C1C=CC=CC=1NN)(O)=O.O.[CH3:24][N:25]([CH3:42])[CH:26]1[CH2:38][C:37]2[C:36]3[C:31](=[C:32]([C:39]([OH:41])=[O:40])[CH:33]=[CH:34][CH:35]=3)[NH:30][C:29]=2[CH2:28][CH2:27]1>C(O)C>[CH3:24][N:25]([CH3:42])[CH:26]1[CH2:38][C:37]2[C:36]3[C:31](=[C:32]([C:39]([OH:41])=[O:40])[CH:33]=[CH:34][CH:35]=3)[NH:30][C:29]=2[CH2:28][CH2:27]1

参加物

5

反応物 3

HCID 104169Benzoic acid, 2-hydrazinyl-, hydrochloride (1:1)HCID 103745454-(Dimethylamino)cyclohexan-1-oneHCID 234703133-(Dimethylamino)-8-carboxy-1,2,3,4-tetrahydrocarbazole hydrate

生成物 1

HCID 128918623-(Dimethylamino)-8-carboxy-1,2,3,4-tetrahydrocarbazole

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution of 14.1 g. of 4-dimethylaminocyclohexanone and 18.9 g. of 2-carboxyphenylhydrazine hydrochloride in 150 ml. of absolute ethyl alcohol was heated under reflux for six hours, cooled, and the resulting crystalline 4-dimethylaminocyclohexanone 2-carboxyphenylhydrazone hydrochloride was collected by filtration, washed with isopropyl alcohol and ether, suspended in 200 ml. of 2% hydrogen chloride in acetic acid and heated at reflux for eight hours. The mixture was cooled and the solids were collected by filtration, washed with isopropyl alcohol and dissolved in 400 ml. of water. The aqueous solution was treated with alkali until neutral and allowed to stand for two hours. The resulting crystals were filtered to give, on recrystallization from water, 30.3 g. of 3-(dimethylamino)-8-carboxy-1,2,3,4-tetrahydrocarbazole hydrate, m.p. >300° C. (dec.)

後処理

  1. temperatureunder reflux for six hours
  2. temperaturecooled
  3. filtrationthe resulting crystalline 4-dimethylaminocyclohexanone 2-carboxyphenylhydrazone hydrochloride was collected by filtration
  4. washwashed with isopropyl alcohol and ether
  5. temperatureof 2% hydrogen chloride in acetic acid and heated
  6. temperatureat reflux for eight hours
  7. temperatureThe mixture was cooled
  8. filtrationthe solids were collected by filtration
  9. washwashed with isopropyl alcohol
  10. dissolutiondissolved in 400 ml
  11. additionThe aqueous solution was treated with alkali until neutral and
  12. filtrationThe resulting crystals were filtered
  13. customto give, on recrystallization from water, 30.3 g

出典と根拠

ORDレコード
ord-aab44a3003df49fea3604fa02382d5b6
出典データセット
uspto-grants-1979_10
特許番号
US04172834

関連ノート

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