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m-Chloroperbenzoic acid → 4-Chloro-3-fluoropyridine 1-oxide

HRID 418054
ノート
印刷プレビュー

反応式

HRID 418054 の反応式
C1C=C(Cl)C=C(C(OO)=[O:9])C=1.[Cl:12][C:13]1[CH:18]=[CH:17][N:16]=[CH:15][C:14]=1[F:19]>C(Cl)Cl>[Cl:12][C:13]1[CH:18]=[CH:17][N+:16]([O-:9])=[CH:15][C:14]=1[F:19]
参加物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 70297m-Chloroperbenzoic acidHCID 38524294-Chloro-3-fluoropyridine

生成物 1

HCID 215698534-Chloro-3-fluoropyridine 1-oxide

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

MCPBA (28.1 g) was added to a solution of 4-chloro-3-fluoro-pyridine (10.0 g) in DCM (150 ml) and the reaction mixture stirred for 60 h at RT. The reaction mixture was quenched with 10% aq. Na2S2O3 and the basicity of the aq. phase adjusted with aq. sat. Na2CO3 to pH 9. The aq. phase was extracted with EA (6×), and the combined org. phase was dried over MgSO4 and evaporated to dryness. The desired compound (8.4 g) was used in the next step without further purification.

後処理

  1. customThe reaction mixture was quenched with 10% aq. Na2S2O3
  2. extractionThe aq. phase was extracted with EA (6×)
  3. dry with materialphase was dried over MgSO4
  4. customevaporated to dryness
  5. customThe desired compound (8.4 g) was used in the next step without further purification

出典と根拠

ORDレコード
ord-7b0b97b2ff0b46f3a7997c171a9aa9f8
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08093250B2

反応ノート

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