聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 3-Pyridinecarbonitrile, 6-(chlorodifluoromethyl)-

温度

100 °C

(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 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.

1. customThe solvent was then removed under reduced pressure
2. dissolutionthe remaining mixture was re-dissolved in DMF (20 mL)
3. extractionthe resulting mixture was extracted with ether-CH2CH2 (1:2
4. washThe combined organic layer was washed with brine
5. customdried
6. filtrationfiltered
7. concentrationconcentrated
8. customThe residue was purified on silica gel

ORD记录

ord-2ef34c23c7cd44458b50514db155b48e

来源数据集

uspto-grants-2013_12

DOI

10.6084/m9.figshare.5104873.v1

专利号

US08598214B2