반응 #640972
ord-08b19a016cad489897ebdc2483198fd2
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상세 조건
See reaction.notes.procedure_details.
후처리
- 1workup.ADDITIONThe reaction mixture were poured into ice-cold aqueous Na2CO3 solution
- 2추출extracted with ethyl acetate
- 3세척The organic layer washed with brine
- 4건조dried over anhydrous Na2SO4
- 5여과filtered
- 6농축concentrated in vacuo
실험 절차
A mixture of NaN3 (481 mg, 7.4 mmol) and 5-[1-chloro-2,2,2-trifluoro-eth-(Z)-ylideneamino]-4′-methyl-biphenyl-3-carboxylic acid methyl ester (1.3 g, 3.7 mmol) in 10 ml of dry ACN was stirred at room temperature for 16 hours. The reaction mixture were poured into ice-cold aqueous Na2CO3 solution, extracted with ethyl acetate. The organic layer washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The resulting crude 4′-methyl-5-(5-trifluoromethyl-tetrazol-1-yl)-biphenyl-3-carboxylic acid methyl ester (1.34 g, 99% yield) was used directly in the next step.