Phenylethanolamine → N-(2-[4-Carbomethoxyphenyl]-1-methylethyl)-2-hydroxy-2-phenylethanamine

HRID 434377ノート

反応式

HRID 434377 の反応式
[OH:1][CH:2]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[CH2:3][NH2:4].[C:11]([C:15]1[CH:20]=[CH:19][C:18]([CH2:21][C:22](=O)[CH3:23])=[CH:17][CH:16]=1)([O:13][CH3:14])=[O:12].CCOCC>C(O)C.[Pd]>[C:11]([C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH:22]([NH:4][CH2:3][CH:2]([OH:1])[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH3:23])=[CH:17][CH:16]=1)([O:13][CH3:14])=[O:12]

参加物

6

反応物 3

HCID 1000PhenylethanolamineHCID 3283Diethyl EtherHCID 11137970Methyl 4-(2-oxopropyl)benzoate

生成物 1

HCID 6917725N-(2-[4-Carbomethoxyphenyl]-1-methylethyl)-2-hydroxy-2-phenylethanamine

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

A mixture of 2-hydroxy-2-phenylethanamine (17.7 g) and 1-(4-carbomethoxyphenyl) propan-2-one (24.8 g) in ethanol (300 ml) was refluxed for one hour. When cooled, 10% Pd/C (1.0 g) was added and the mixture was hydrogenated on a Parr Hydrogenator at 60° and 60 psi for six hours. The mixture was filtered and the filtrate was evaporated to an oil which was taken up in methanol (75 ml). The solution was allowed to stand at 4° to give crystals (Batch 1). Ether (75 ml) was added to the mother liquors to obtain subsequent crops (Batches 2 & 3). The mother liquors were evaporated to an oil, which was crystallised from ether (Batch 4).

後処理

  1. temperaturewas refluxed for one hour
  2. temperatureWhen cooled
  3. customwas hydrogenated on a Parr Hydrogenator at 60°
  4. filtrationThe mixture was filtered
  5. customthe filtrate was evaporated to an oil which
  6. customto stand at 4°
  7. customto give crystals (Batch 1)
  8. customto obtain subsequent crops (Batches 2 & 3)
  9. customThe mother liquors were evaporated to an oil, which
  10. customwas crystallised from ether (Batch 4)

出典と根拠

ORDレコード
ord-995f7563b6c844b0836fa583cba53dd3
出典データセット
uspto-grants-1983_08
特許番号
US04396627

反応ノート

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