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Allyl bromide → Methyl 4-(3-bromopropyl)benzoate

HRID 352607
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반응식

HRID 352607 반응식
[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][CH2:12]O)=[CH:6][CH:5]=1.C(N1C=CN=C1)(N1C=CN=C1)=O.C([Br:30])C=C>CC#N>[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][CH2:12][Br:30])=[CH:6][CH:5]=1
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참가 물질

5

반응물 3

HCID 7841Allyl bromideHCID 682631,1'-CarbonyldiimidazoleHCID 14425137Methyl 4-(3-hydroxypropyl)benzoate

생성물 1

HCID 10801120Methyl 4-(3-bromopropyl)benzoate

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A solution of 4-(3-hydroxy-propyl)-benzoic acid methyl ester (11.98 g) and 1,1′-carbonyldiimidazole (9.0 g, 55.50 mmol) in CH3CN (200 mL) was stirred at room temperature for 1.5 h. Allyl bromide (20 mL) was added and the reaction mixture was heated under reflux for 20 h. The reaction mixture was cooled to room temperature and saturated aqueous NaHCO3was added. The aqueous solution was washed with EtOAc (3×) and the organic solutions were combined, dried (MgSO4), filtered and concentrated. Purification by medium pressure chromatography (9:1 hexanes:EtOAc) provided the title compound of Preparation 4.

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureunder reflux for 20 h
  3. additionsaturated aqueous NaHCO3was added
  4. washThe aqueous solution was washed with EtOAc (3×)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurification by medium pressure chromatography (9:1 hexanes:EtOAc)
  9. customprovided

출처 및 근거

ORD 기록
ord-5b30b649f6b44b599e105f5a025099ed
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06747054B2

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