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Sodium Hydroxide → Furo[3,2-c]pyridin-6-ylmethanol

HRID 1383003
ノート
印刷プレビュー

反応式

HRID 1383003 の反応式
[OH2:1].[CH3:2][C:3]1[N+:8]([O-])=[CH:7][C:6]2[CH:10]=[CH:11][O:12][C:5]=2[CH:4]=1.[OH-].[Na+]>C(OC(=O)C)(=O)C.Cl>[OH:1][CH2:2][C:3]1[N:8]=[CH:7][C:6]2[CH:10]=[CH:11][O:12][C:5]=2[CH:4]=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

5

反応物 2

HCID 14798Sodium HydroxideHCID 21273331HCID 21273331、化合物

生成物 1

HCID 14005234Furo[3,2-c]pyridin-6-ylmethanol収率 64%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 7918Acetic Anhydride溶媒

反応条件

温度
100 °C

実験手順

A mixture of 6-methylfuro[3,2-c]pyridine-N-oxide monohydrate (19.85 g, 0.119 mol) in acetic anhydride (30 mL) was heated at 100° C. for one half hour. Then the reaction mixture was diluted with 20% hydrochloric acid (100 mL) and heating was continued for one hour. The solution was cooled and made basic with sodium hydroxide solution. The product was extracted into chloroform, dried over anhydrous sodium sulfate, filtered through a pad of charcoal and evaporated. The residue was triturated with cool benzene and the crystalline product collected by filtration to give 11.36 g (64% yield), mp: 72°-74° C.

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

後処理

  1. temperatureheating
  2. temperatureThe solution was cooled
  3. extractionThe product was extracted into chloroform
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered through a pad of charcoal
  6. customevaporated
  7. customThe residue was triturated with cool benzene
  8. filtrationthe crystalline product collected by filtration
  9. customto give 11.36 g (64% yield), mp: 72°-74° C.

出典と根拠

ORDレコード
ord-a409d72270784fcf98f40e0d728af78f
出典データセット
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04808595

反応ノート

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