Hydrochloric Acid → (R)-N-(2-((10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)methoxy)ethyl)-3-piperidinecarboxylic acid hydrochloride

HRID 2226753ノート

反応式

HRID 2226753 の反応式
C([O:3][C:4]([C@@H:6]1[CH2:11][CH2:10][CH2:9][N:8]([CH2:12][CH2:13][O:14][CH:15]=[C:16]2[C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=3[CH2:20][CH2:19][C:18]3[CH:27]=[CH:28][CH:29]=[CH:30][C:17]2=3)[CH2:7]1)=[O:5])C.[OH-].[Na+].O.[ClH:34]>C(O)C.ClCCl>[ClH:34].[CH:27]1[C:18]2[CH2:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[C:16](=[CH:15][O:14][CH2:13][CH2:12][N:8]3[CH2:9][CH2:10][CH2:11][C@@H:6]([C:4]([OH:5])=[O:3])[CH2:7]3)[C:17]=2[CH:30]=[CH:29][CH:28]=1

参加物

7

反応条件

温度
50 °C

実験手順

The above ester (2.0 g, 4.9 mmol) was dissolved in ethanol (20 ml) and a 4 N sodium hydroxide solution (4.9 ml) was added. The mixture was stirred at 50° C. for 2 h. Water (10 ml) was added and ethanol was evaporated in vacuo to give an aqueous residue. A 4 M aqueous hydrochloric acid solution (6.2 ml) was added followed by dichloromethane (50 ml). The phases were separated and the aqueous phase was extracted with dichloromethane (50 ml). The combined organic phases were washed with water (10 ml) and then dried over magnesium sulphate. The solvent was evaporated in vacuo and the residue dried in vacuo to give 1.71 g of the title compound as a solid.

後処理

  1. customethanol was evaporated in vacuo
  2. customto give an aqueous residue
  3. customThe phases were separated
  4. extractionthe aqueous phase was extracted with dichloromethane (50 ml)
  5. washThe combined organic phases were washed with water (10 ml)
  6. dry with materialdried over magnesium sulphate
  7. customThe solvent was evaporated in vacuo
  8. customthe residue dried in vacuo

出典と根拠

ORDレコード
ord-e012b1090b164fa18eb7f4f26ba53a68
出典データセット
uspto-grants-1994_09
特許番号
US05348965

反応ノート

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