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2,4-Dihydroxybenzaldehyde → 2-hydroxy-4-(3methylbut-2-enyloxy)benzaldehyde

HRID 1603167
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HRID 1603167 반응식
[OH-].[K+].[OH:3][C:4]1[CH:11]=[C:10]([OH:12])[CH:9]=[CH:8][C:5]=1[CH:6]=[O:7].[CH3:13][C:14]([CH3:18])=[CH:15][CH2:16]Br>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.C(OCC)(=O)C>[CH3:13][C:14]([CH3:18])=[CH:15][CH2:16][O:12][C:10]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[C:4]([OH:3])[CH:11]=1
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참가 물질

6

반응물 3

HCID 72132,4-DihydroxybenzaldehydeHCID 14797Potassium HydroxideHCID 700922-Butene, 1-bromo-3-methyl-

생성물 1

HCID 108674672-hydroxy-4-(3methylbut-2-enyloxy)benzaldehyde수율 17.3%

시약·촉매·용매 2

HCID 66133Benzyl triethylammonium chloride촉매HCID 8857
Ethyl Acetate
용매

실험 절차

A solution of 6 g (0.11 mol) of potassium hydroxide, 22.7 g (0.1 mol) of benzyltriethylammonium chloride, and 14 g (0.1 mol) of 2,4-dihydroxybenzaldehyde was concentrated in vacuo. The residue was suspended in 100 ml of ethyl acetate and 11.7 ml (0.1 mol) of dimethylallyl bromide was slowlv added to the solution. The mixture was extracted with 100 ml of water, and the organic phase was dried and concentrated in vacuo to give 3.568 g of a residue, from which 4.738 g (20%) of 4-(3-methyl)-but-2-enyloxy-2-hydroxybenzaldehyde identical to that previously described by S. Khan, and M. Krishnamurti in Indian J. Chem. 22B (1983), 276 was purified by column chromatography over silica gel 60 (Merck 0.063-0.200 mm, 200 g) using petroleum ether-ethyl acetate (9:1) as an eluent.

후처리

  1. extractionThe mixture was extracted with 100 ml of water
  2. customthe organic phase was dried
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-5e2fcd4e4b66447baf30e2a412b4e875
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05985935

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