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m-Chloroperbenzoic acid → 2-Bromo-5-methylpyridine 1-oxide

HRID 541422
ノート
印刷プレビュー

反応式

HRID 541422 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][N:3]=1.C1C=C(Cl)C=C(C(OO)=[O:17])C=1>ClCCl.[OH-].[Na+]>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][N+:3]=1[O-:17]
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 70297m-Chloroperbenzoic acidHCID 5642162-Bromo-5-methylpyridine

生成物 1

HCID 131787372-Bromo-5-methylpyridine 1-oxide

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 14798Sodium Hydroxide溶媒2 回

反応条件

温度
30 °C

実験手順

Into a round-bottom flask, was placed a solution of 2-bromo-5-methylpyridine (10.0 g, 58.1 mmol, 1.00 equiv) in dichloromethane (250 mL). mCPBA (15.0 g, 86.9 mmol, 1.50 equiv) was added in several batches at room temperature. The resulting solution was stirred overnight at 30° C., then diluted with 50 mL of 2N sodium hydroxide (aq.). The pH value of the solution was adjusted to 10 with 2N sodium hydroxide (aq.). The aqueous phase was extracted with 3×100 mL of dichloromethane and the combined organic layers were dried over anhydrous magnesium sulfate and concentrated under reduced pressure to yield 11.0 g (91%) of 2-bromo-5-methylpyridin-1-ium-1-olate as a yellow solid.

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. customInto a round-bottom flask, was placed
  2. extractionThe aqueous phase was extracted with 3×100 mL of dichloromethane
  3. dry with materialthe combined organic layers were dried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customto yield 11.0 g (91%) of 2-bromo-5-methylpyridin-1-ium-1-olate as a yellow solid

出典と根拠

ORDレコード
ord-dd0389c101d74488b83f58d19e2af4bc
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871790B2

反応ノート

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