Ethyl 2-chloroacetoacetate → HCID 69280529, 화합물
반응식
[F:1][C:2]1[C:10]([F:11])=[C:9]([C:12]([F:15])([F:14])[F:13])[CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[S:5].Cl[CH:17]([C:23]([CH3:25])=O)[C:18]([O:20][CH2:21][CH3:22])=[O:19]>C(O)C>[CH2:21]([O:20][C:18]([C:17]1[S:5][C:4]([C:3]2[CH:7]=[CH:8][C:9]([C:12]([F:15])([F:14])[F:13])=[C:10]([F:11])[C:2]=2[F:1])=[N:6][C:23]=1[CH3:25])=[O:19])[CH3:22]참가 물질
4
실험 절차
A solution of 2,3-difluoro-4-trifluoromethyl-thiobenzamide (1.15 g, 4.8 mmol) and ethyl 2-chloro-acetoacetate (0.67 ml, 4.8 mmol) in ethanol (70 ml) was heated at reflux temperature for 14 hours. The solvent was removed under reduced pressure and the residue partitioned between ice water and ethyl acetate. The layers were separated and the aqueous phase extracted two more times with ethyl acetate. The combined extracts were washed two times with ice water/brine 1/1 and dried over sodium sulfate. The solvent was removed under reduced pressure to give a yellow oil which was purified by column chromatography (silica gel, heptane/AcOEt) to yield 700 mg (2 mmol, 42%) of the title compound as yellow crystals.
후처리
- temperatureat reflux temperature for 14 hours
- customThe solvent was removed under reduced pressure
- customthe residue partitioned between ice water and ethyl acetate
- customThe layers were separated
- extractionthe aqueous phase extracted two more times with ethyl acetate
- washThe combined extracts were washed two times with ice water/brine 1/1
- dry with materialdried over sodium sulfate
- customThe solvent was removed under reduced pressure
- customto give a yellow oil which
- customwas purified by column chromatography (silica gel, heptane/AcOEt)
출처 및 근거
- ORD 기록
- ord-eee3dc61cd5d4a0997248e0ee4608ce4
- 출처 데이터셋
- uspto-grants-2007_06
- 특허 번호
- US07235572B2
반응 노트
불러오는 중…