Thiophosgene → 5-Fluoro-o-tolyl Isothiocyanate

HRID 1372654

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HRID 1372654 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:9])=[C:6]([CH:8]=1)[NH2:7].C(=O)([O-])[O-].[Ca+2].[C:15](Cl)(Cl)=[S:16].C(Cl)Cl.O>C(Cl)Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:9])=[C:6]([N:7]=[C:15]=[S:16])[CH:8]=1

참가 물질

6

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온도
0 °C

실험 절차

Under stirring at 0° C., a solution of 5-fluoro-2-methylaniline (1.23 g, 9.84 mmol) in methylene chloride (10 ml) was added dropwise to a mixture of calcium carbonate (2.46 g, 24.6 mmol) and thiophosgene (750 μl, 9.84 mmol) in a methylene chloride/water (1/1, 40 ml) mixture. After completion of the dropwise addition, the reaction mixture was stirred further at 0° C. for 35 minutes. The reaction mixture was poured in ice-1N HCR, followed by extraction with chloroform. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent to give 5-fluoro-2-methylphenyl isothiocyanate (1.45 g, 88%) as a brown oil.

후처리

  1. additionAfter completion of the dropwise addition
  2. stirringthe reaction mixture was stirred further at 0° C. for 35 minutes
  3. extractionfollowed by extraction with chloroform
  4. washThe extract was washed with saturated brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationdistilled under reduced pressure
  7. customto remove the solvent

출처 및 근거

ORD 기록
ord-90810f355c7b4e559e01de12d40ed540
출처 데이터셋
uspto-grants-2007_01
특허 번호
US07157487B2

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