반응 #65265
ord-36b0a4d7b9a846cf893de012bb3b71a0
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후처리
- 1기타The resulting solid mass was sonicated
- 2기타to form a suspension
- 3기타The ice bath was removed
- 4기타the reaction mixture was irradiated for 20 hours with a 450-watt mercury vapor lamp
- 5온도cooled
- 6온도The reaction mixture was cooled to -20° C.
- 7추출The product was extracted into ethyl acetate (3×)
- 8세척the combined extracts were washed with water and saturated sodium chloride solution
- 9추출The organic extract
- 10건조was dried with anhydrous sodium sulfate
- 11농축concentrated
- 12기타to give 8.43 g of a crude product, which
- 13기타was chromatographed on silica gel eluting with chloroform
실험 절차
The 4-amino product was fluorinated using the procedure of K. L. Kirk and L. J. Cohen, JACS, 95 (14), 4619 (1973). Fluoroboric acid (48%, 150 mL) was added to 2-n-butyl-1-{(2-chlorophenyl)methyl}-4-amino-5-carboethoxyimidazole (10.75 g, 0.032 mol) in a quartz flask. The resulting solid mass was sonicated and stirred vigorously to form a suspension. This suspension was cooled to 0° C. and then sodium nitrite (2.80 g, 0.0406 mol) in 5 mL of water was added slowly. The ice bath was removed and then the reaction mixture was irradiated for 20 hours with a 450-watt mercury vapor lamp placed in a quartz immersion well, cooled by circulating water. The reaction mixture was cooled to -20° C. and the pH was adjusted to 6.4 with 50% aqueous sodium hydroxide. The product was extracted into ethyl acetate (3×) and the combined extracts were washed with water and saturated sodium chloride solution. The organic extract was dried with anhydrous sodium sulfate and concentrated to give 8.43 g of a crude product, which was chromatographed on silica gel eluting with chloroform to give 4.31 g of 2-n-butyl-1-{(2-chlorophenyl)methyl}-4-fluoro-5-carboethoxyimidazole.