Ammonia → 4-Amino-3,5-dichlorobenzotrifluoride

HRID 1018176

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HRID 1018176 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:10]([F:13])([F:12])[F:11])[CH:5]=[C:6]([Cl:9])[C:7]=1Cl.[F-].[Li+].[NH3:16]>CN1CCCC1=O>[Cl:1][C:2]1[CH:3]=[C:4]([C:10]([F:13])([F:12])[F:11])[CH:5]=[C:6]([Cl:9])[C:7]=1[NH2:16]

참가 물질

5

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온도
-95 °C

실험 절차

3,4,5-Trichloro-trifluoromethylbenzene (0.681 g, 2.73 mmol), lithium fluoride (7.1 mg, 0.273 mmol) and N-methylpyrrolidone (1.8 ml) are mixed in an autoclave. The autoclave is cooled to −95° C. and then ammonia (1.3 g, 76.4 mmol) is added. The autoclave is then heated at 250° C. and with stirring for 4 h and is subsequently allowed to return to room temperature. The reaction product is extracted by washing with water and with dichloromethane and then the organic phase is evaporated, after having been dried. 0.453 g (1.97 mmol) of 2,6-dichloro-4-trifluoromethylaniline is obtained with a degree of conversion of the 3,4,5-trichloro-trifluoromethylbenzene of 97%, a ratio equal to 83/17 for the selectivity for 2,6-dlchloro-para-trifluoromethylaniline with respect to 2,6-dichloro-meta-trifluoromethylaniline and an 87% yield of 2,6-dichloro-para-trifluoromethylaniline.

후처리

  1. temperatureThe autoclave is then heated at 250° C.
  2. customto return to room temperature
  3. extractionThe reaction product is extracted
  4. washby washing with water and with dichloromethane
  5. customthe organic phase is evaporated
  6. customafter having been dried

출처 및 근거

ORD 기록
ord-6475831cd98b4b2986b7ef106e72a8e5
출처 데이터셋
uspto-grants-2002_11
특허 번호
US06479703B1

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