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

HRID 1603167
ノート
印刷プレビュー

反応式

HRID 1603167 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 66133Benzyl triethylammonium chloride触媒HCID 8857
Ethyl Acetate
溶媒

実験手順

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.

後処理

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

出典と根拠

ORDレコード
ord-5e2fcd4e4b66447baf30e2a412b4e875
出典データセット
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05985935

反応ノート

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