Sulfuric Acid → 5-Hydroxy-1-methyl-5-(3-methylphenyl)pyrrolidin-2-one

HRID 268286노트

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HRID 268286 반응식
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

참가 물질

7

실험 절차

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.

후처리

  1. temperaturerefluxed for about 4 hours
  2. stirringStirring
  3. temperatureto maintain a gentle reflux
  4. waitAfter an additional 0.5 hours
  5. customthe water layer is separated
  6. washwashed twice with 50 ml
  7. washwashed with 50 ml
  8. dry with materialThe resulting layer is dried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. customevaporated in vacuo
  11. customThe resulting residue is crystallized from methylene chloride/hexane

출처 및 근거

ORD 기록
ord-b2d07190ad0845dd98bbc3e2d03676ca
출처 데이터셋
uspto-grants-1976_03
특허 번호
US03947460

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