4,6-Dibromoisochroman-1-one → 6-bromo-1H-isochromen-1-one
反応式
Br[CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Br:12])[CH:10]=2)[C:5](=[O:13])[O:4][CH2:3]1>C(Cl)Cl>[Br:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[C:5](=[O:13])[O:4][CH:3]=[CH:2]2参加物
3
実験手順
4,6-Dibromo-3,4-dihydro-1H-isochromen-1-one (1.8 g, 5.8 mmol) was dissolved in DCM (15 ml) then added TEA (20 mL, 143 mmol) and stirred at room temperature for 72 hours. The mixture was concentrated then took up the residue with DCM and washed with 1N HCl. Repeated the wash with brine then dried over Na2SO4 and evaporated to dryness. The residue was purified by MPLC with 0-100% EtOAc/hexane to yield 6-Bromo-1H-isochromen-1-one. LC-MS (IE, m/z): 227 [M+2]+.
後処理
- concentrationThe mixture was concentrated
- washwashed with 1N HCl
- washwash with brine
- dry with materialthen dried over Na2SO4
- customevaporated to dryness
- customThe residue was purified by MPLC with 0-100% EtOAc/hexane
出典と根拠
- ORDレコード
- ord-0a2346eee1314b6580262ec231704e21
- 出典データセット
- uspto-grants-2015_04
- 特許番号
- US08999990B2
反応ノート
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