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

HRID 1825039
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인쇄 미리보기

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HRID 1825039 반응식
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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8083MorpholineHCID 748703-BromostyreneHCID 86662868Sodium t-butyloxide

생성물 1

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

시약·촉매·용매 2

HCID 167845palladium(II) acetate촉매HCID 6344Dichloromethane용매

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온도
80 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-0f3ebebc36514c95ab35d3c792e48e40
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045551B2

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