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4-bromo-N-methoxy-N,3-dimethylbenzamide → 1-(4-Bromo-3-methyl-phenyl)-5-methyl-hexan-1-one

HRID 1669328
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HRID 1669328 반응식
[Br:1][C:2]1[CH:13]=[CH:12][C:5]([C:6](N(OC)C)=[O:7])=[CH:4][C:3]=1[CH3:14]>O1CCCC1>[Br:1][C:2]1[CH:13]=[CH:12][C:5]([C:6](=[O:7])[CH2:12][CH2:13][CH2:2][CH:3]([CH3:14])[CH3:4])=[CH:4][C:3]=1[CH3:14]
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참가 물질

3

반응물 1

HCID 218337954-bromo-N-methoxy-N,3-dimethylbenzamide

생성물 1

HCID 673424431-(4-Bromo-3-methyl-phenyl)-5-methyl-hexan-1-one수율 159.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

4-Bromo-N-methoxy-3,N-dimethyl-benzamide (5.94 g, 23.05 mmol) was suspended in anhydrous tetrahydrofuran (200 mL), and cooled to 0° C. with stirring under nitrogen. 1-magnesium bromo-4-methyl-pentane (23 mL, 1.5M in tetrahydrofuran, 34.8 mmol) was slowly added to the reaction over 1 h. The reaction was allowed to warm slowly to room temperature and monitored by TLC. Upon complete consumption of starting material, the reaction was carefully neutralized with 1N hydrochloric acid, extracted with diethyl ether, washed, dried, and concentrated. The 1-(4-Bromo-3-methyl-phenyl)-5-methyl-hexan-1-one (5.2 g, 18.4 mmol) 80% yield, was used without further purification.

후처리

  1. temperatureto warm slowly to room temperature
  2. customUpon complete consumption of starting material
  3. extractionextracted with diethyl ether
  4. washwashed
  5. customdried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-3ce2a462c65c4d16842640066d971750
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07989457B2

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