p-Toluenesulfonic acid → Benzyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate

HRID 1395482

反応式

HRID 1395482 の反応式
[CH:1]([CH:14]1[CH2:19][CH2:18][N:17]([C:20](=[O:27])[CH2:21][O:22][CH2:23][C:24]([OH:26])=[O:25])[CH2:16][CH2:15]1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:28]1([CH3:38])[CH:33]=[CH:32][C:31](S(O)(=O)=O)=[CH:30][CH:29]=1>C(O)C1C=CC=CC=1>[CH:1]([CH:14]1[CH2:15][CH2:16][N:17]([C:20](=[O:27])[CH2:21][O:22][CH2:23][C:24]([O:26][CH2:38][C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)=[O:25])[CH2:18][CH2:19]1)([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

参加物

4

反応物 2

HCID 6101p-Toluenesulfonic acidHCID 196442Mcn 4308

生成物 1

HCID 54337918Benzyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate

試薬・触媒・溶媒 1

HCID 244Benzyl Alcohol溶媒

実験手順

In a similar operation, 3.63 grams (10 millimoles) of [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetic acid, 50 milliliters of benzyl alcohol and 150 milligrams of p-toluenesulfonic acid are mixed together and the resulting mixture heated at reflux temperature for about 6 hours to obtain a product in the reaction mixture. Thereafter, the reaction mixture subjected to reduced pressure to evaporate the alcohol and the residue is dissolved in benzene, the resulting solution washed with bicarbonate solution, dried and the solvent evaporated to obtain a benzyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate product. The molecular weight of benzyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate is 453.

後処理

  1. temperaturethe resulting mixture heated
  2. temperatureat reflux temperature for about 6 hours
  3. customto obtain a product in the reaction mixture
  4. customto evaporate the alcohol
  5. dissolutionthe residue is dissolved in benzene
  6. washthe resulting solution washed with bicarbonate solution
  7. customdried
  8. customthe solvent evaporated

出典と根拠

ORDレコード
ord-f2d81979881a46fe8cff0aac2c8f1a3c
出典データセット
uspto-grants-1980_05
特許番号
US04203991

関連ノート

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