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Hydrochloric Acid → 3-Trifluoromethyl-4-phenyl-5-chloroisoxazole

HRID 477392
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HRID 477392 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[C:6](N)[O:5][N:4]=1.[ClH:17].[N+]([O-])([O-])=O.[Na+]>O>[F:1][C:2]([F:16])([F:15])[C:3]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[C:6]([Cl:17])[O:5][N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 24268Sodium NitrateHCID 156138913-Trifluoromethyl-4-phenyl-5-aminoisoxazole

생성물 1

HCID 143710873-Trifluoromethyl-4-phenyl-5-chloroisoxazole수율 16.9%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To 2.28 g (10.0 mmole) of 3-trifluoromethyl-4-phenyl-5-aminoisoxazole were added 20 ml of conc. HCl and 1.09 g (11. 0 mmole) of cuprous chloride and 4.2 ml of aqueous sodium nitrate (2.76 g, 40 mmole) was added dropwise to the reaction mixture, keeping the temperature at 20°-25° C. After addition, the temperature was raised to 40°-45° C. and the mixture was stirred for 1 hour. To the mixture was added 16 ml of water, extracted with methylene chloride, dried with anhydrous sodium sulfate, evaporated under reduced pressure. The residue was purified by chromatography on silica gel to give 0.5651 g of colorless liquid. This was distilled under reduced pressure to give 0.4193 g of the titled compound as colorless liquid, yield 16.9%, b.p. 80.0°-83.0° C./0.50 mmHg.

후처리

  1. additionwas added dropwise to the reaction mixture
  2. customat 20°-25° C
  3. additionAfter addition
  4. temperaturethe temperature was raised to 40°-45° C.
  5. extractionextracted with methylene chloride
  6. dry with materialdried with anhydrous sodium sulfate
  7. customevaporated under reduced pressure
  8. customThe residue was purified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-9a2637dc85144ca5a8eb66c8d453f4e8
출처 데이터셋
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04888044

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