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

HRID 2421846
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HRID 2421846 반응식
[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]
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참가 물질

4

반응물 1

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

생성물 1

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

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

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온도
70 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-217da6b6e262468e83e12698184952bb
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07960376B2

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