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Methyl iodide → (5S)-5-(p-toluenesulphonylmethyl)-1-methyl-2-pyrrolidinone

HRID 454316
Notes
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Reaction equation

HRID 454316 reaction equation
[C:1]1([CH3:17])[CH:6]=[CH:5][C:4]([S:7]([CH2:10][C@H:11]2[NH:15][C:14](=[O:16])[CH2:13][CH2:12]2)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[CH:18]([N-]C(C)C)(C)C.[Li+].CI>C1COCC1>[C:1]1([CH3:17])[CH:2]=[CH:3][C:4]([S:7]([CH2:10][C@H:11]2[N:15]([CH3:18])[C:14](=[O:16])[CH2:13][CH2:12]2)(=[O:9])=[O:8])=[CH:5][CH:6]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 2724682Lithium diisopropylamideHCID 11242222HCID 11242222, compound

Product 1

HCID 57001804(5S)-5-(p-toluenesulphonylmethyl)-1-methyl-2-pyrrolidinoneYield 40%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-70 °C

Procedure

(5S)-5-(p-Toluenesulphonylmethyl)-2-pyrrolidinone (0.8 g, 3 mmol) was dissolved in dry THF and cooled to −70° C. Lithium diisopropylamide was slowly added and the reaction stirred for 20 minutes before addition of methyl iodide (2 ml, excess). The reaction was allowed to warm to ambient temperature for over 2 hours. The reaction was partitioned between ethyl acetate and water, the organic layer separated, dried over MgSO4, filtered, and evaporated in vacuo. The residue was purified by flash chromatography eluting from methylene chloride to 5% methanol/95% methylene chloride and the product evaporated to give (5S)-5-(p-toluenesulphonyl-methyl)-1-methyl-2-pyrrolidinone (340 mg, 40%) as a brown oil.

Workup

  1. temperatureto warm to ambient temperature for over 2 hours
  2. customThe reaction was partitioned between ethyl acetate and water
  3. customthe organic layer separated
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customThe residue was purified by flash chromatography
  8. washeluting from methylene chloride to 5% methanol/95% methylene chloride
  9. customthe product evaporated

Sources & evidence

ORD record
ord-1bee2935a2fb43a0abf794641a963d96
Source dataset
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08492560B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes