反応式
Br[C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][C@@H:8]([CH2:11][OH:12])[O:7][C:6]=2[CH:13]=1.[CH3:14][S:15]([O-:17])=[O:16].[Na+].N1CCC[C@H]1C(O)=O.C([O-])([O-])=O.[K+].[K+]>CS(C)=O.[Cu]I>[CH3:14][S:15]([C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][C@@H:8]([CH2:11][OH:12])[O:7][C:6]=2[CH:13]=1)(=[O:17])=[O:16]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
Two batches of [(2R)-7-bromo-2,3-dihydro-1,4-benzodioxin-2-yl]methanol (2.2 g, 8.9 mmol), sodium methanesulfinate (85%) (1.6 g, 13.3 mmol), CuI (0.2 g, 0.9 mmol), L-proline (0.2 g, 1.8 mmol) and K2CO3 (0.2 g, 1.8 mmol) in DMSO (20 ml) were heated under microwave radiation at 140° C. for 3 h in nitrogen-flushed vials. Water and EtOAc were added. The water layer was extracted with EtOAc (3×100 ml) and the combined organic phases were washed with LiCl (5%), HCl (1 N) and brine. The resulting solution was dried (Na2SO4) and evaporated to dryness. The residue was purified by flash column chromatography (isooctane/EtOAc) to give the title compound (1.7 g). MS m/z (rel. intensity, 70 eV) 244 (M+, bp), 213 (39), 165 (26), 134 (22), 79 (23).
後処理
- customflushed vials
- additionWater and EtOAc were added
- extractionThe water layer was extracted with EtOAc (3×100 ml)
- washthe combined organic phases were washed with LiCl (5%), HCl (1 N) and brine
- dry with materialThe resulting solution was dried (Na2SO4)
- customevaporated to dryness
- customThe residue was purified by flash column chromatography (isooctane/EtOAc)
出典と根拠
- ORDレコード
- ord-4c5db21f63e6492c829c6c16c4269287
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524766B2
関連ノート
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