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Water → 3-(3-Chlorophenoxy)nitrobenzene

HRID 49433
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HRID 49433 반응식
CC(C)([O-])C.[K+].[Cl:7][C:8]1[CH:9]=[C:10]([OH:14])[CH:11]=[CH:12][CH:13]=1.F[C:16]1[CH:17]=[C:18]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:20][CH:21]=1.O>CS(C)=O>[Cl:7][C:8]1[CH:9]=[C:10]([CH:11]=[CH:12][CH:13]=1)[O:14][C:16]1[CH:17]=[C:18]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:20][CH:21]=1
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참가 물질

6

반응물 4

HCID 962WaterHCID 79333-ChlorophenolHCID 98231-Fluoro-3-nitrobenzeneHCID 23665647Potassium tert-butoxide

생성물 1

HCID 221751693-(3-Chlorophenoxy)nitrobenzene

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

To a stirred solution of potassium t-butoxide (12.3 g) in DMSO (100 mL) was added at once 3-chlorophenol (12.86 g). The resulting solution was stirred for 5 minutes at room temperature, then 3-fluoronitrobenzene (12.70 g) was added all at once. The resulting dark mixture was heated at 120° C. for 12 hours, cooled to room temperature then poured into water (700 mL). The resulting mixture was extracted with ether (2×200 mL). The organic fraction was washed with 2N NaOH (100 mL), then with water (100 mL). After drying (MgSO4), the solvent was evaporated and the resulting dark oil was distilled to give 3-(3-chlorophenoxy)nitrobenzene as a yellow oil, b.p. 135-140° C. at 0.05 mm.

후처리

  1. temperatureThe resulting dark mixture was heated at 120° C. for 12 hours
  2. temperaturecooled to room temperature
  3. extractionThe resulting mixture was extracted with ether (2×200 mL)
  4. washThe organic fraction was washed with 2N NaOH (100 mL)
  5. dry with materialAfter drying (MgSO4)
  6. customthe solvent was evaporated
  7. distillationthe resulting dark oil was distilled

출처 및 근거

ORD 기록
ord-89cc7c7040e5453ca0c9c3c22b33282b
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706740B2

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