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Sodium Thiosulfate → 2-Chloro-3-(1-fluorocyclobutyl)-6-methylpyridine 1-oxide

HRID 624993
ノート
印刷プレビュー

反応式

HRID 624993 の反応式
ClC1C=C(C=CC=1)C(OO)=[O:6].[Cl:12][C:13]1[C:18]([C:19]2([F:23])[CH2:22][CH2:21][CH2:20]2)=[CH:17][CH:16]=[C:15]([CH3:24])[N:14]=1.[O-]S([O-])(=S)=O.[Na+].[Na+]>ClCCl>[Cl:12][C:13]1[C:18]([C:19]2([F:23])[CH2:22][CH2:21][CH2:20]2)=[CH:17][CH:16]=[C:15]([CH3:24])[N+:14]=1[O-:6]
参加物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 24477Sodium ThiosulfateHCID 70297m-Chloroperbenzoic acidHCID 902024992-Chloro-3-(1-fluorocyclobutyl)-6-methylpyridine

生成物 1

HCID 902025652-Chloro-3-(1-fluorocyclobutyl)-6-methylpyridine 1-oxide収率 75%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

3-Chlorobenzoperoxoic acid (173 mg, 1.00 mmol) was added in 2 portions to a solution of 2-chloro-3-(1-fluorocyclobutyl)-6-methylpyridine (Example 130 b, 100 mg, 501 μmol) in dichloromethane (2 mL). The reaction mixture was stirred at ambient temperature for 72 h, poured onto a 10% aqueous Na2S2O3 solution (30 mL) and extracted with dichloromethane (2×40 mL). The combined organic layers were washed with ice water/brine (30 mL), dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in dichloromethane, washed with sat. NaHCO3 solution (30 mL) and ice water (30 mL), dried over Na2SO4 and concentrated in vacuo to give the title compound (81 mg, 74%) as yellow oil, MS (ESI): m/e=216.3 [MH+].

後処理

  1. extractionextracted with dichloromethane (2×40 mL)
  2. washThe combined organic layers were washed with ice water/brine (30 mL)
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. dissolutionThe residue was dissolved in dichloromethane
  6. washwashed with sat. NaHCO3 solution (30 mL) and ice water (30 mL)
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-9e6f35e3eddb4e7cb0b3b8c060ba9254
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09303012B2

反応ノート

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