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Potassium Nitrate → 4-Tert-butyl-2-chloro-5-nitrophenyl methyl carbonate

HRID 423816
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반응식

HRID 423816 반응식
[C:1](=[O:16])([O:14][CH3:15])[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([CH3:12])([CH3:11])[CH3:10])=[CH:5][C:4]=1[Cl:13].[N+:17]([O-])([O-:19])=[O:18].[K+]>OS(O)(=O)=O>[C:1](=[O:16])([O:14][CH3:15])[O:2][C:3]1[CH:8]=[C:7]([N+:17]([O-:19])=[O:18])[C:6]([C:9]([CH3:11])([CH3:12])[CH3:10])=[CH:5][C:4]=1[Cl:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24434Potassium NitrateHCID 574702304-Tert-butyl-2-chlorophenyl methyl carbonate

생성물 1

HCID 574702314-Tert-butyl-2-chloro-5-nitrophenyl methyl carbonate수율 2,740.6%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

4-tert-Butyl-2-chlorophenyl methyl carbonate (36.0 g, 0.15 mol) was dissolved in conc. H2SO4 (100 mL) at 0° C. KNO3 (0.53 g, 5.2 mmol) was added in portions over 25 min. The reaction was stirred for 1.5 h and poured into ice (200 g). The aqueous layer was extracted with dichloromethane. The combined organic layers were washed with aq. NaHCO3, dried over Na2SO4 and concentrated under vacuum to give 4-tert-butyl-2-chloro-5-nitrophenyl methyl carbonate (41.0 g), which was used without further purification.

후처리

  1. extractionThe aqueous layer was extracted with dichloromethane
  2. washThe combined organic layers were washed with aq. NaHCO3
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-6d22ccdfe9df4030b2117596bf16c74d
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08101767B2

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