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Water → 3-(3-Chlorophenoxy)nitrobenzene

HRID 49433
ノート
印刷プレビュー

反応式

HRID 49433 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

HCID 221751693-(3-Chlorophenoxy)nitrobenzene

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-89cc7c7040e5453ca0c9c3c22b33282b
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06706740B2

反応ノート

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