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Formaldehyde → Benzenemethanol,2-hydroxy-3,5-dimethyl-

HRID 371147
ノート
印刷プレビュー

反応式

HRID 371147 の反応式
[CH2:1]=[O:2].[CH3:3][C:4]1[CH:9]=[C:8]([CH3:10])[CH:7]=[CH:6][C:5]=1[OH:11].[OH-].[Na+]>O>[CH3:3][C:4]1[CH:9]=[C:8]([CH3:10])[CH:7]=[C:6]([CH2:1][OH:2])[C:5]=1[OH:11]
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

5

反応物 3

HCID 712FormaldehydeHCID 77712,4-DimethylphenolHCID 14798Sodium Hydroxide2 回

生成物 1

HCID 11480550Benzenemethanol,2-hydroxy-3,5-dimethyl-

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
50 °C

実験手順

A 38% solution of formaldehyde (32.0 grams, 0.4 mol) was added to a stirred solution of 2,4-dimethylphenol (36.6 grams, 0.3 mol) in water (100 ml) containing sodium hydroxide (14 gr., 0.35 mol) and heated at 50° C. for 4 to 5 hours. The reaction was cooled and solid sodium hydroxide added to precipitate the salt of the product. The solid was removed by filtration and dissolved in water. This solution was neutralized with carbon dioxide (dry ice) and the resulting mixture was extracted with methylene chloride. The organic layer was removed, dried, and evaporated to yield a light brown solid. This solid was washed in hexane containing a small amount of toluene to afford a tan solid. The NMR1 and FD/MS2 data support the structure.

後処理

  1. temperatureThe reaction was cooled
  2. customto precipitate the salt of the product
  3. customThe solid was removed by filtration
  4. dissolutiondissolved in water
  5. extractionthe resulting mixture was extracted with methylene chloride
  6. customThe organic layer was removed
  7. customdried
  8. customevaporated
  9. customto yield a light brown solid
  10. washThis solid was washed in hexane containing a small amount of toluene
  11. customto afford a tan solid

出典と根拠

ORDレコード
ord-ee33765bf3bb4c019e4bcc67e00f7ef4
出典データセット
uspto-grants-1985_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04529533

反応ノート

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