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Trifluoroacetic acid → 2-Cyclohexyl-8-methyl-4-oxo-4H-[1]-benzopyran

HRID 1200183
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반응식

HRID 1200183 반응식
[CH:1]1([C:7](=[O:19])[CH2:8][C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH3:17])[C:12]=2O)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.FC(F)(F)C(O)=O>ClCCl>[CH:1]1([C:7]2[O:19][C:12]3[C:13]([CH3:17])=[CH:14][CH:15]=[CH:16][C:11]=3[C:9](=[O:10])[CH:8]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 146504291-Cyclohexyl-3-(2-hydroxy-3-methylphenyl)-1,3-propanedione

생성물 1

HCID 146504342-Cyclohexyl-8-methyl-4-oxo-4H-[1]-benzopyran

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1-Cyclohexyl-3-(2-hydroxy-3-methylphenyl)-1,3-propanedione (5.2 g) was dissolved in dichloromethane (50 ml). Trifluoroacetic acid (4 ml) was added to the solution and the mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure and then extracted with ethyl acetate. The extract was washed with water, saturated aqueous sodium bicarbonate and then water and dried (MgSO4). The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate (4:1)) to obtain the title compound as crystals. The crystals were recrystallized from ethyl acetate and hexane to obtain prisms (3.66 g), m.p. 108°-109° C., yield 75.6%.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with water, saturated aqueous sodium bicarbonate
  4. dry with materialwater and dried (MgSO4)
  5. distillationThe solvent was distilled off under reduced pressure
  6. customthe residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate (4:1))

출처 및 근거

ORD 기록
ord-f9f0d87207d7426686ccc4a3656c0ae0
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04904690

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