Sulfuric Acid → 5-Hydroxy-1-methyl-5-(3-methylphenyl)pyrrolidin-2-one
反応式
Br[C:2]1[CH:3]=[C:4]([CH3:8])[CH:5]=[CH:6][CH:7]=1.[Mg].[CH3:10][N:11]1[C:15](=[O:16])[CH2:14][CH2:13][C:12]1=[O:17].S(=O)(=O)(O)O>C1C=CC=CC=1.C(OCC)C>[OH:16][C:15]1([C:2]2[CH:3]=[C:4]([CH3:8])[CH:5]=[CH:6][CH:7]=2)[N:11]([CH3:10])[C:12](=[O:17])[CH2:13][CH2:14]1参加物
実験手順
To a Grignard prepared from 27.3g (0.16 mole) of 3-bromotoluene and 3.7 g. (0.16 mole) of magnesium turnings in 100 ml. of dry diethylether, there is added dropwise over a period of about 10 minutes 12.2 g. (0.11 mole) of N-methylsuccinimide in 100 ml. of dry benzene. The resulting mixture is stirred and refluxed for about 4 hours and then allowed to stand overnight at room temperature. Stirring is resumed and 40 ml. of 50% sulfuric acid is added dropwise at such a rate to maintain a gentle reflux. After an additional 0.5 hours, the water layer is separated and washed twice with 50 ml. of benzene. The organic layers are combined and washed with 50 ml. of sodium carbonate and then twice more with 50 ml. of water. The resulting layer is dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The resulting residue is crystallized from methylene chloride/hexane to give 5-hydroxy-1-methyl-5-(m-tolyl) pyrrolidone; m.p. 128°-130°C.
後処理
- temperaturerefluxed for about 4 hours
- stirringStirring
- temperatureto maintain a gentle reflux
- waitAfter an additional 0.5 hours
- customthe water layer is separated
- washwashed twice with 50 ml
- washwashed with 50 ml
- dry with materialThe resulting layer is dried over anhydrous magnesium sulfate
- filtrationfiltered
- customevaporated in vacuo
- customThe resulting residue is crystallized from methylene chloride/hexane
出典と根拠
- ORDレコード
- ord-b2d07190ad0845dd98bbc3e2d03676ca
- 出典データセット
- uspto-grants-1976_03
- 特許番号
- US03947460
反応ノート
読み込み中…