반응 #46904
ord-efdd765be6a748e18147c7442f20519c
반응 방정식
반응 조건
후처리
- 1workup.STIRRINGstirred for 1 h at 0° C.
- 2기타at room temperature
- 3여과After filtration
- 4기타the filtrate was evaporated under reduced pressure
- 5기타the oily residue thus obtained
- 6세척the organic layer was washed with brine
- 7건조dried on anhydrous MgSO4
- 8여과filtered
- 9기타the solvent evaporated
- 10세척eluted with CH2Cl2/MeOH (9/1), from which 4-carbamoylphenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate (5)
- 11기타was obtained (212 mg, 17% yield)
실험 절차
To the solution of 1 (diclofenac, 890 mg, 3.0 mmol) in 50 mL of N,N-dimethylformamide, hydroxybenzotriazole (445 mg, 3.3 mmol) and DCC (680 mg, 3.3 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxybenzamide (4, 616 mg, 4.5 mmol) was added and stirred for 1 h at 0° C. and 3 hs at room temperature. After filtration, the filtrate was evaporated under reduced pressure and the oily residue thus obtained was dissolved in chloroform; the organic layer was washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 5 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9/1), from which 4-carbamoylphenyl 2-(2-(2,6-dichlorophenylamino)phenyl)acetate (5) was obtained (212 mg, 17% yield).