Water → HCID 86631570、化合物

To 21 mL of a 1M tetrahydrofuran solution of 1-trifluoromethylethenyl zinc bromide prepared according to a method described in the literatures, a solution of 2.4 g of 4-bromo-2,6-dichloro(difluoromethoxy)benzene in 12 mL of N,N-dimethylformamide was added, and tetrahydrofuran was distilled off under reduced pressure. To the remaining N,N-dimethylformamide solution, 0.23 g of dichlorobis(triphenylphosphine) palladium (II) was added and the resultant mixture was stirred at 100° C. for 3 hours. After the completion of the reaction, the reaction mixture was left to be cooled down to room temperature and charged into 100 mL of water and the resultant mixture was extracted with diethyl ether (100 mL×1). The organic phase was washed with water and then dehydrated and dried over saturated saline and anhydrous sodium sulfate in this order and the solvent was distilled off under reduced pressure. The resultant residue was purified by silica gel column chromatography eluting with hexane to obtain 1.8 g of the objective substance as a brown oily substance.

1. distillationtetrahydrofuran was distilled off under reduced pressure
2. additionTo the remaining N,N-dimethylformamide solution, 0.23 g of dichlorobis(triphenylphosphine) palladium (II) was added
3. customAfter the completion of the reaction
4. waitthe reaction mixture was left
5. temperatureto be cooled down to room temperature
6. extractionthe resultant mixture was extracted with diethyl ether (100 mL×1)
7. washThe organic phase was washed with water
8. dry with materialdried over saturated saline and anhydrous sodium sulfate in this order
9. distillationthe solvent was distilled off under reduced pressure
10. customThe resultant residue was purified by silica gel column chromatography
11. washeluting with hexane
12. customto obtain 1.8 g of the objective substance as a brown oily substance

ORDレコード

ord-2aa98a461fd64f7a8dbbb2af06e61cd7

出典データセット

uspto-grants-2012_11

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08318757B2