反応 #3443
ord-ddd7e0bd7cef44e8b59de3a93c55dc2b
反応方程式
溶媒
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他The product was purified by chromatography over silica gel eluting with 20% EtOAc/hexane
実験手順
1-([1,1'-Biphenyl]-3-ylmethyl)-4-hydroxy-2-methyl-1H-indole (1.03 g, 3.3 mmol) was alkylated by treating with 0.31 mL (3.3 mmol) of methyl bromoacetate and 132 mg (3.3 mmol) of 60% NaH/mineral oil in DMF as described in Example 1, Part E. The product was purified by chromatography over silica gel eluting with 20% EtOAc/hexane, to give 1.0 g (79% yield) of [[1-([1,1'-biphenyl]-3-ylmethyl)-2-methyl-1H-indol-4-yl]oxy]acetic acid methyl ester, 99°-102° C.