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Acetic Anhydride → 2-Hydroxymethyl-3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine

HRID 727764
ノート
印刷プレビュー

反応式

HRID 727764 の反応式
[CH3:1][C:2]1[C:7]([CH3:8])=[C:6]([O:9][CH2:10][C:11]([F:17])([F:16])[C:12]([F:15])([F:14])[F:13])[CH:5]=[CH:4][N+:3]=1[O-].C(OC(=O)C)(=[O:21])C>S(=O)(=O)(O)O>[OH:21][CH2:1][C:2]1[C:7]([CH3:8])=[C:6]([O:9][CH2:10][C:11]([F:17])([F:16])[C:12]([F:15])([F:14])[F:13])[CH:5]=[CH:4][N:3]=1
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

4

反応物 2

HCID 7918Acetic AnhydrideHCID 136547942,3-Dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide

生成物 1

HCID 136547662-Hydroxymethyl-3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid触媒

反応条件

温度
110 °C

実験手順

Concentrated sulfuric acid (2 drops) was added to a solution of 2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine-1-oxide (2.5 g) in acetic anhydride (8 ml) and the mixture was stirred at 110° C. for 2 hours and then concentrated. The residue was dissolved in methanol (30 ml), 2 N aqueous sodium hydroxide (20 ml) was added, and the mixture was stirred at room temperature for 2 hours. After concentration, water was added to the residue and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate, the solvent was then distilled off, and the residue was applied to a silica gel (50 g) column. Elution with chloroform-methanol (10:1) and recrystallization from isopropyl ether gave 1.6 g of 2-hydroxymethyl-3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine as a brown oil.

後処理

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in methanol (30 ml)
  3. addition2 N aqueous sodium hydroxide (20 ml) was added
  4. stirringthe mixture was stirred at room temperature for 2 hours
  5. concentrationAfter concentration, water
  6. additionwas added to the residue
  7. extractionthe mixture was extracted with ethyl acetate
  8. dry with materialThe extract was dried over magnesium sulfate
  9. distillationthe solvent was then distilled off
  10. washElution
  11. customwith chloroform-methanol (10:1) and recrystallization from isopropyl ether

出典と根拠

ORDレコード
ord-08f10c0f110e47ceb42c8649bab4ac45
出典データセット
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05045321

反応ノート

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