反応式
[Cl:1][C:2]([F:11])([F:10])[C:3](=O)/[CH:4]=[CH:5]/OCC.C[N:13](C)[CH:14]=[CH:15][C:16]#[N:17].C([O-])(=O)C.[NH4+].O>C1(C)C=CC=CC=1>[Cl:1][C:2]([F:10])([F:11])[C:3]1[CH:4]=[CH:5][C:15]([C:16]#[N:17])=[CH:14][N:13]=1参加物
反応条件
- 温度
- 100 °C
実験手順
(3E)-1-Chloro-4-ethoxy-1,1-difluorobut-3-en-2-one (7.36 g, 40 mmol) was dissolved in dry toluene (40 mL) and treated with 3-dimethylaminoacrylonitrile (4.61 g, 48 mmol) at room temperature. The solution was heated at about 100° C. for 3.5 hr. The solvent was then removed under reduced pressure and the remaining mixture was re-dissolved in dimethyl formamide (DMF; 20 mL), treated with ammonium acetate (4.62 g, 60 mmol) and stirred at room temperature overnight. Water was added to the reaction mixture and the resulting mixture was extracted with ether-CH2CH2 (1:2, v/v) twice. The combined organic layer was washed with brine, dried, filtered and concentrated. The residue was purified on silica gel to give 3.1 g of 6-[chloro(difluoro)methyl]nicotinonitrile (A) as light colored oil in 41% yield. GC-MS: mass calcd for C7H3ClF2N2 [M]+ 188. Found 188.
後処理
- customThe solvent was then removed under reduced pressure
- dissolutionthe remaining mixture was re-dissolved in dimethyl formamide (DMF; 20 mL)
- extractionthe resulting mixture was extracted with ether-CH2CH2 (1:2
- washThe combined organic layer was washed with brine
- customdried
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified on silica gel
出典と根拠
- ORDレコード
- ord-55356535618a4eb08c6dbf33cd6b9f14
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08188292B2
関連ノート
読み込み中…