Hydrochloric Acid → HCID 86643611, 화합물

HRID 570683노트

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HRID 570683 반응식
[F:1][C:2]([F:13])([F:12])[CH2:3][O:4][C:5]1[CH:11]=[CH:10][C:8]([NH2:9])=[CH:7][CH:6]=1.Cl.[C:15](Cl)(Cl)=[S:16].C(=O)([O-])O.[Na+]>O1CCCC1>[N:9]([C:8]1[CH:10]=[CH:11][C:5]([O:4][CH2:3][C:2]([F:12])([F:13])[F:1])=[CH:6][CH:7]=1)=[C:15]=[S:16]

참가 물질

6

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온도
-5 °C

실험 절차

4-(2,2,2-Trifluoroethoxy)aniline (10 g) was dissolved in tetrahydrofuran (100 ml), 6M hydrochloric acid (9 ml) was added thereto, and the mixture was cooled to −5° C. A solution of thiophosgene (4.01 ml) in tetrahydrofuran (20 ml) was added dropwise thereto over 5 min, and the mixture was stirred at −5° C. for 10 min. Saturated aqueous sodium hydrogen carbonate solution (125 ml) was poured into the mixture, and the mixture was extracted twice with ethyl acetate (200 ml). The extracted layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the obtained brown crude product was purified by silica gel column chromatography, and the obtained pale-yellow solid was washed with hexane to give the title compound (10.7 g) as white crystals.

후처리

  1. extractionthe mixture was extracted twice with ethyl acetate (200 ml)
  2. washwashed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure
  5. customthe obtained brown crude product was purified by silica gel column chromatography
  6. washthe obtained pale-yellow solid was washed with hexane

출처 및 근거

ORD 기록
ord-cfac4f2acc164909b993835ffb2cad14
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09023858B2

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