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Diisobutylaluminum hydride → ((1r)-1-Phenylethyl){[3-(4-methoxyphenyl)-4-methylphenyl]methyl}amine

HRID 1072250
ノート
印刷プレビュー

反応式

HRID 1072250 の反応式
[C:1]1([C@H:7]([NH:9][C:10]([C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[C:14]([C:19]3[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=3)[CH:13]=2)=O)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[C:1]1([C@H:7]([NH:9][CH2:10][C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[C:14]([C:19]3[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=3)[CH:13]=2)[CH3:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1.[C:1]1([C@H:7]([NH:9][CH2:10][C:12]2[CH:17]=[CH:16][C:15]([CH3:18])=[C:14]([C:19]3[CH:20]=[CH:21][C:22]([OH:25])=[CH:23][CH:24]=3)[CH:13]=2)[CH3:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14487Diisobutylaluminum hydrideHCID 20803221n-((1r)-1-Phenylethyl)[3-(4-methoxyphenyl)-4-methylphenyl]carboxamide

生成物 2

HCID 60010447((1r)-1-Phenylethyl){[3-(4-methoxyphenyl)-4-methylphenyl]methyl}amineHCID 600105454-(5-{[((1r)-1-Phenylethyl)amino]methyl}-2-methylphenyl)phenol

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a solution of N-((1R)-1-phenylethyl)[3-(4-methoxyphenyl)-4-methylphenyl]carboxamide (0.12 g, 0.34 mmol) in 10 mL of toluene was added DIBAL-H (1 mL, 1.5 mmol). The reaction was then heated to 100 C. for 16 hours and cooled to RT. The reaction was quenched with 5 mL of 2N NaOH aq. soln. 100 mL of CH2Cl2 was used to extract the product. The organic phase was washed with 30 mL of brine, dried over Na2SO3 and concentrated in vacuo. The desired products were separated by silica gel column chromatography (30% to 60% EtOAc in hexane) provide ((1R)-1-phenylethyl){[3-(4-methoxyphenyl)-4-methylphenyl]methyl}amine and 4-(5-{[((1R)-1-phenylethyl)amino]methyl}-2-methylphenyl)phenol, which were treated with 1N HCl in Et2O separately to provide the HCl salts as white solids.

後処理

  1. temperatureThe reaction was then heated to 100 C
  2. customThe reaction was quenched with 5 mL of 2N NaOH aq. soln
  3. extractionto extract the product
  4. washThe organic phase was washed with 30 mL of brine
  5. dry with materialdried over Na2SO3
  6. concentrationconcentrated in vacuo
  7. customThe desired products were separated by silica gel column chromatography (30% to 60% EtOAc in hexane)

出典と根拠

ORDレコード
ord-a31d1a22c4ba4ce093da60519111af73
出典データセット
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06908935B2

反応ノート

読み込み中…

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