ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Methyl 4-(4-chloro-2-methylbutan-2-ylthio)-3-nitrobenzoate → Methyl 3-amino-4-(4-chloro-2-methylbutan-2-ylthio)benzoate

HRID 2421846
ノート
印刷プレビュー

反応式

HRID 2421846 の反応式
[Cl:1][CH2:2][CH2:3][C:4]([CH3:20])([S:6][C:7]1[CH:16]=[CH:15][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:9][C:8]=1[N+:17]([O-])=O)[CH3:5]>CC(O)=O.[Fe]>[NH2:17][C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][C:7]=1[S:6][C:4]([CH3:20])([CH2:3][CH2:2][Cl:1])[CH3:5])[C:11]([O:13][CH3:14])=[O:12]
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 1

HCID 67242953Methyl 4-(4-chloro-2-methylbutan-2-ylthio)-3-nitrobenzoate

生成物 1

HCID 67242880Methyl 3-amino-4-(4-chloro-2-methylbutan-2-ylthio)benzoate

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 176Acetic Acid溶媒

反応条件

温度
70 °C

実験手順

To a solution of methyl 4-(4-chloro-2-methylbutan-2-ylthio)-3-nitrobenzoate (3.43 g, 10.8 mmol) in AcOH (100 mL) was added iron (2.413 g, 43.2 mmol). The reaction was heated to 70° C. and stirred at that temperature for 2 hours. The solvent was removed under reduced pressure and the resulting paste was diluted with H2O (250 mL). The solution was treated with K3PO4 until pH=6. The aqueous layer was extracted with EtOAc (3×150 mL). The combined organics were washed with saturated aqueous NaHCO3 (50 mL) and brine (50 mL) then dried over Na2SO4 and concentrated in vacuo. The product was isolated as a brown solid and used without further purification.

後処理

  1. customThe solvent was removed under reduced pressure
  2. additionthe resulting paste was diluted with H2O (250 mL)
  3. additionThe solution was treated with K3PO4 until pH=6
  4. extractionThe aqueous layer was extracted with EtOAc (3×150 mL)
  5. washThe combined organics were washed with saturated aqueous NaHCO3 (50 mL) and brine (50 mL)
  6. dry with materialthen dried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. customThe product was isolated as a brown solid
  9. customused without further purification

出典と根拠

ORDレコード
ord-217da6b6e262468e83e12698184952bb
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07960376B2

反応ノート

読み込み中…

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