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Benzyl Bromide → 4-Benzyloxy-benzenesulfonic acid 4-amino-3-nitrophenyl ester

HRID 1823777
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HRID 1823777 반응식
C(=O)([O-])[O-].[Cs+].[Cs+].[NH2:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][S:15]([C:18]2[CH:23]=[CH:22][C:21]([OH:24])=[CH:20][CH:19]=2)(=[O:17])=[O:16])=[CH:10][C:9]=1[N+:25]([O-:27])=[O:26].[CH2:28](Br)[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>O.CN(C)C=O>[NH2:7][C:8]1[CH:13]=[CH:12][C:11]([O:14][S:15]([C:18]2[CH:19]=[CH:20][C:21]([O:24][CH2:28][C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)=[CH:22][CH:23]=2)(=[O:16])=[O:17])=[CH:10][C:9]=1[N+:25]([O-:27])=[O:26]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7498Benzyl BromideHCID 10796Cesium carbonateHCID 86596077HCID 86596077, 화합물

생성물 1

HCID 865960764-Benzyloxy-benzenesulfonic acid 4-amino-3-nitrophenyl ester

시약·촉매·용매 2

HCID 962Water용매2회HCID 6228Dimethylformamide용매

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온도
80 °C

실험 절차

A solution of cesium carbonate (156 mg) in water (0.3 ml) was added to a solution of 4-hydroxy-benzenesulfonic acid 4-amino-3-nitro-phenyl ester (150 mg) and benzyl bromide (58 μl) in dimethylformamide (3 ml). The reaction mixture was heated at 80° C. for 3 hours then allowed to cool to ambient temperature, poured into water (25 ml) and extracted three times with ethyl acetate (30 ml). The combined extracts were dried over magnesium sulfate then evaporated to give 189 mg of crude 4-benzyloxy-benzenesulfonic acid 4-amino-3-nitrophenyl ester.

후처리

  1. temperatureto cool to ambient temperature
  2. extractionextracted three times with ethyl acetate (30 ml)
  3. dry with materialThe combined extracts were dried over magnesium sulfate
  4. customthen evaporated

출처 및 근거

ORD 기록
ord-a7bed9eaf87e4e62adec3d48e60a22ab
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07041668B2

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