Sodium Hypochlorite → HCID 86608017、化合物
反応式
[CH2:1]([S:3][C:4](SCC)=[C:5]([C:19]([F:22])([F:21])[F:20])[CH2:6][C:7]([C:9]1[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=1)=[O:8])[CH3:2].[O-:26]Cl.[Na+]>C(O)(C(F)(F)F)=O.O>[CH2:1]([S:3][C:4](=[O:26])[CH:5]([C:19]([F:22])([F:21])[F:20])[CH2:6][C:7](=[O:8])[C:9]1[CH:14]=[CH:13][C:12]([C:15]([F:18])([F:17])[F:16])=[CH:11][CH:10]=1)[CH3:2]参加物
5
実験手順
A mixture of 4,4-bis-ethylsulfanyl-3-trifluoromethyl-1-(4-trifluoromethyl-phenyl)-but-3-en-1-one (example C.26 step 3) (36.96 g, 92 mmol) in TFA (54.3 mL) and water (5.8 mL) was refluxed for 18 h under nitrogen atmosphere, the exhaust of the reaction was passed through a NaOCl solution to trap the liberated ethyl mercaptane. The volatiles were evaporated and the mixture was diluted with water and extracted with TBME, the organic layer was washed with sat. NaHCO3-sol. and brine, dried over Na2SO4. Removal of the solvent in vacuum left the title compound as a brown oil (31.2 g, 95%), which was used without further purification [according to J. Fluorine Chem. 2001, 107, 281. ]. MS (EI) 339.0 [(M−F)+].
後処理
- temperaturewas refluxed for 18 h under nitrogen atmosphere
- customThe volatiles were evaporated
- additionthe mixture was diluted with water
- extractionextracted with TBME
- washthe organic layer was washed with sat. NaHCO3-sol
- dry with materialand brine, dried over Na2SO4
- customRemoval of the solvent in vacuum
- waitleft the title compound as a brown oil (31.2 g, 95%), which
- customwas used without further purification [according to J. Fluorine Chem. 2001, 107, 281. ]
出典と根拠
- ORDレコード
- ord-2528249965b44952b50871c29566971e
- 出典データセット
- uspto-grants-2008_11
- 特許番号
- US07446113B2
反応ノート
読み込み中…