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Potassium Iodide → 2-Methyl-4-[(prop-2-en-1-yl)oxy]benzaldehyde

HRID 892256
ノート
印刷プレビュー

反応式

HRID 892256 の反応式
C(=O)([O-])[O-].[K+].[K+].[I-].[K+].[OH:9][C:10]1[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[C:12]([CH3:18])[CH:11]=1.[CH2:19](Br)[CH:20]=[CH2:21]>CC(=O)CC>[CH2:21]([O:9][C:10]1[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[C:12]([CH3:18])[CH:11]=1)[CH:20]=[CH2:19]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 4875Potassium IodideHCID 7841Allyl bromideHCID 11430Potassium CarbonateHCID 4581854-Hydroxy-2-methylbenzaldehyde

生成物 1

HCID 222420922-Methyl-4-[(prop-2-en-1-yl)oxy]benzaldehyde収率 98%

試薬・触媒・溶媒 1

HCID 6569Methyl Ethyl Ketone溶媒

反応条件

温度
65 °C

実験手順

31.7 g (229 mmol) potassium carbonate and 9.51 g (57.3 mmol) potassium iodide were given to a solution of 15.6 g (115 mmol) 4-hydroxy-2-methyl-benzaldehyde and 55.4 g (458 mmol) allyl bromide in 500 ml 2-butanone and stirred for 16 h at 65° C. Solvents were distilled off and the residue distributed between ethyl acetate and 1 N sodium hydroxide. The organic layer was separated and the aqueous solution extracted once with ethyl acetate. The combined organic phases were dried and evaporated to give 19.8 g (98%) of 4-allyloxy-2-methyl-benzaldehyde.

後処理

  1. distillationSolvents were distilled off
  2. customThe organic layer was separated
  3. extractionthe aqueous solution extracted once with ethyl acetate
  4. customThe combined organic phases were dried
  5. customevaporated

出典と根拠

ORDレコード
ord-18bf9a3d06064dd9baa6dd02eb02cf3b
出典データセット
uspto-grants-2006_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07005526B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート