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Acetone → 2,4-Bis(allyloxy)benzaldehyde

HRID 394960
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HRID 394960 반응식
[OH:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].Br[CH2:12][CH:13]=[CH2:14].C(=O)([O-])[O-].[K+].[K+].[CH3:21][C:22]([CH3:24])=O>>[CH2:12]([O:1][C:2]1[CH:9]=[C:8]([O:10][CH2:24][CH:22]=[CH2:21])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5])[CH:13]=[CH2:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 180AcetoneHCID 72132,4-DihydroxybenzaldehydeHCID 7841Allyl bromideHCID 11430Potassium Carbonate

생성물 1

HCID 51824082,4-Bis(allyloxy)benzaldehyde수율 93%

실험 절차

To a solution of 6.9 g (50 mmol) of 2,4-dihydroxybenzaldehyde in 100 ml of acetone was added 12 ml (120 mmol) of 3-bromopropene and 40 g of potassium carbonate and the mixture was refluxed for 3 h under stirring. The mixture was filtered and the filtrate concentrated in vacuo to give 10.2 g (93%) of 2,4-diprop-2-enyloxybenzaldehyde as slightly reddish crystals.

후처리

  1. temperaturethe mixture was refluxed for 3 h
  2. filtrationThe mixture was filtered
  3. concentrationthe filtrate concentrated in vacuo

출처 및 근거

ORD 기록
ord-b4afe83461064144a8ba926fc5539048
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06603046B1

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