反応式
[O:1]1[C:6]2[CH:7]=[CH:8][C:9](C=O)=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1.[OH:13]S(O)(=O)=O.OO>>[OH:13][C:9]1[CH:8]=[CH:7][C:6]2[O:1][CH2:2][CH2:3][O:4][C:5]=2[CH:10]=1参加物
4
実験手順
1,4-Benzodioxan-6-carboxaldehyde (5.20 g) was dissolved in MeCH (60 mL) containing conc. H2SO4 (0.6 mL). At 0° C. an aqueous solution of 30% H2O2 (4.7 mL) was added to the mixture over 5 minutes. The mixture was warmed to room temperature, stirred an additional 18 h and evaporated. The residue was taken up with H2O and extracted with CH2Cl2. The extract was dried (Na2SO4), filtered and evaporated. The residue was purified by column chromatography (silica gel; eluent: hexane to hexane/EtOAc 3:1) to give 6-hydroxy-1,4-benzodioxan (3.85 g). ESMS: m/z 153 MH+.
後処理
- customevaporated
- extractionextracted with CH2Cl2
- dry with materialThe extract was dried (Na2SO4)
- filtrationfiltered
- customevaporated
- customThe residue was purified by column chromatography (silica gel; eluent: hexane to hexane/EtOAc 3:1)
出典と根拠
- ORDレコード
- ord-0b2fe497114b490485af30fa6dd42043
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06855843B2
関連ノート
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