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4-(Trifluoromethyl)aniline → HCID 11301521, 화합물

HRID 898823
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HRID 898823 반응식
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1.[C:12]([N:17]1[CH2:21][CH2:20][O:19][C:18]1=[O:22])(=[O:16])/[CH:13]=[CH:14]/[CH3:15].[Cl-].[NH4+]>C1(C)C=CC=CC=1>[F:1][C:2]([F:10])([F:11])[C:3]1[CH:9]=[CH:8][C:6]([NH:7][CH:14]([CH3:15])[CH2:13][C:12]([N:17]2[CH2:21][CH2:20][O:19][C:18]2=[O:22])=[O:16])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 99644-(Trifluoromethyl)anilineHCID 25517Ammonium ChlorideHCID 53658453-[(E)-2-Butenoyl]-1,3-oxazolidin-2-one

생성물 1

HCID 11301521HCID 11301521, 화합물수율 75.3%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of 4-trifluoromethylaniline (193 mg, 1.2 mmol) and 3-crotonoyl-1,3-oxazolidin-2-one (155 mg, 1.0 mmol) in toluene (3 ml) in a stream of nitrogen was added Pd((R)-binap)(H2O)2(OTf)2 (26.6 mg, 0.025 mmol) and the resulting mixture was stirred at room temperature for 16 hours. After completion of the reaction, a saturated aqueous solution of ammonium chloride (10 ml) was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate (10 ml). The organic layer was dried over anhydrous magnesium sulfate. The solvent was then evaporated off and the crude product obtained was purified by a silica gel column chromatography (hexane:ethyl acetate=1:1) to give the objective compound 3-(4-trifluoromethylanilino)butyryl-1,3-oxazolidin-2-one (238 mg, 75% yield). Enantiomeric excess ratio of this product was determined by a liquid chromatography using a column for separation of optical isomers (column: AD-H) to be 83% e.e.

후처리

  1. customAfter completion of the reaction
  2. extractionthe resulting mixture was extracted with ethyl acetate (10 ml)
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. customThe solvent was then evaporated off
  5. customthe crude product obtained
  6. customwas purified by a silica gel column chromatography (hexane:ethyl acetate=1:1)

출처 및 근거

ORD 기록
ord-c2539e421c084425899c51982ee7f755
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07351849B2

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