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Morpholine → 4-(3-Vinyl-phenyl)-morpholine

HRID 1825039
ノート
印刷プレビュー

反応式

HRID 1825039 の反応式
Br[C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[CH2:6].[NH:10]1[CH2:15][CH2:14][O:13][CH2:12][CH2:11]1.C(OC(C)(C)C)(C)(C)C.[Na]>ClCCl.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH:5]([C:4]1[CH:3]=[C:2]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[CH:9]=[CH:8][CH:7]=1)=[CH2:6]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 8083MorpholineHCID 748703-BromostyreneHCID 86662868Sodium t-butyloxide

生成物 1

HCID 221449744-(3-Vinyl-phenyl)-morpholine

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 6344Dichloromethane溶媒

反応条件

温度
80 °C

実験手順

Mixture of 3-bromo-styrene (11.2 g, 61.2 mmol), morpholine (123 mL), palladium acetate (343 mg, 2.5 mol %), di-t-butyl-biphenylphosphine (911 mg, 5 mol %), sodium t-butyloxide (6.47 g, 67.4 mmol) was stirred at 80° C. in a sealed tube for 30 minutes. After cooling down, the reaction mixture was diluted with dichloromethane (250 mL) and washed with water (100 mL). The aqueous layer was extracted with dichloromethane (2×125 mL) and the combined organic layer was dried over magnesium sulfate and concentrated under vacuum. The crude product was purified by Flash Chromatography of Biotage with 30% Ethyl Acetate/Hexanes. The title compound was obtained as pale yellow clear oil (10.7 g, 93% yield).

後処理

  1. temperatureAfter cooling down
  2. washwashed with water (100 mL)
  3. extractionThe aqueous layer was extracted with dichloromethane (2×125 mL)
  4. dry with materialthe combined organic layer was dried over magnesium sulfate
  5. concentrationconcentrated under vacuum
  6. customThe crude product was purified by Flash Chromatography of Biotage with 30% Ethyl Acetate/Hexanes

出典と根拠

ORDレコード
ord-0f3ebebc36514c95ab35d3c792e48e40
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07045551B2

反応ノート

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