反応 #56743
ord-47a056a1e72946a8b88e47f96aa55b91
反応方程式
反応物
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1ろ過The mixture was then filtered through celite and
- 2濃縮concentrated in vacuum
- 3その他chromatographed on silica gel with first 10% hexane/methylene chloride
実験手順
A mixture of 3.75 g (9.2 mmole) of [(2R)-7-nitro-8-(2-oxoethyl)-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate and 3.0 g of platinum oxide in 50 mL of ethyl acetate was treated with 45 psi of hydrogen on a Parr hydrogenation apparatus for 6 hours. The mixture was then filtered through celite and concentrated in vacuum. The residue was column chromatographed on silica gel with first 10% hexane/methylene chloride, then 1% methanol/methylene chloride and finally 2% methanol/methylene chloride to give 1.50 g of the (R)-enantiomer of the title compound as a white solid one-quarter hydrate, m.p. 145° C.