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

HRID 2421845
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반응식

HRID 2421845 반응식
[Cl:1][CH2:2][CH2:3][C:4]([CH3:19])([S:6][C:7]1[CH:15]=[CH:14][C:10]([C:11](Cl)=[O:12])=[CH:9][C:8]=1[N+:16]([O-:18])=[O:17])[CH3:5].C(N(CC)CC)C.[CH3:27][OH:28]>>[Cl:1][CH2:2][CH2:3][C:4]([CH3:19])([S:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([O:28][CH3:27])=[O:12])=[CH:9][C:8]=1[N+:16]([O-:18])=[O:17])[CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 8471TriethylamineHCID 86628743HCID 86628743, 화합물

생성물 1

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

실험 절차

To a solution of 4-(4-chloro-2-methylbutan-2-ylthio)-3-nitrobenzoyl chloride (3.48 g, 10.8 mmol) in MeOH (200 mL) was added triethylamine (15.05 mL, 108 mmol). The reaction was stirred at room temperature for 3 hours. The solvent was removed under reduced pressure. The resulting paste was diluted with EtOAc (200 mL) and washed with saturated aqueous NaHCO3 (75 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The resulting solid was used without further purification.

후처리

  1. customThe solvent was removed under reduced pressure
  • additionThe resulting paste was diluted with EtOAc (200 mL)
  • washwashed with saturated aqueous NaHCO3 (75 mL)
  • dry with materialThe organic layer was dried over Na2SO4
  • concentrationconcentrated in vacuo
  • customThe resulting solid was used without further purification
  • 출처 및 근거

    ORD 기록
    ord-50eb4fa0580f489bac3c4157ca4fd66c
    출처 데이터셋
    uspto-grants-2011_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07960376B2

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