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1,3-Dibromopropane → 3-Allyl-4-(3-bromopropoxy)benzaldehyde

HRID 361708
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HRID 361708 반응식
[Br:1][CH2:2][CH2:3][CH2:4]Br.C(=O)([O-])[O-].[K+].[K+].[CH2:12]([C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][C:22]=1[OH:23])[CH:18]=[O:19])[CH:13]=[CH2:14]>CC(C)=O>[CH2:12]([C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][C:22]=1[O:23][CH2:4][CH2:3][CH2:2][Br:1])[CH:18]=[O:19])[CH:13]=[CH2:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80011,3-DibromopropaneHCID 11430Potassium CarbonateHCID 47290143-Allyl-4-hydroxybenzaldehyde

생성물 1

HCID 539738933-Allyl-4-(3-bromopropoxy)benzaldehyde

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

1,3-Dibromopropane (15.76 ml) and potassium carbonate (4.69 g) were added to a solution of 3-allyl-4-hydroxybenzaldehyde (5 g) in acetone and the reaction mixture heated at reflux for 16 hours. The reaction mixture was cooled to ambient temperature and filtered. The filtrate was evaporated and the residue purified by flash column chromatography on silica gel (Merck Art No 9385) using a 10:90 (v/v) mixture of ethyl acetate/hexane as eluent to give 3-allyl-4-(3-bromopropoxy)benzaldehyde (4.86 g) as an oil which slowly solidified. NMR([CD3 ]2SO): 2.2-2.4(2H,m), 3.35-3.50(2H,m), 3.65-3.80(2H,t), 4.2-4.3(2H,t), 5.0-5.15(2H,m), 5.8-6.1(1H,m), 7.15-7.25(1H,d), 7.7(1H,d), 7.75-7.85(1H,q) and 9,85(1H,s).

후처리

  1. temperaturethe reaction mixture heated
  2. temperatureat reflux for 16 hours
  3. filtrationfiltered
  4. customThe filtrate was evaporated
  5. customthe residue purified by flash column chromatography on silica gel (Merck Art No 9385)
  6. additiona 10:90 (v/v) mixture of ethyl acetate/hexane as eluent

출처 및 근거

ORD 기록
ord-84219d9be37a442fa1ce8c6e3c548024
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05866611

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