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Potassium Carbonate → 1-(4-(2-Hydroxyethyl)phenyl)pyrrolidin-2-one

HRID 1023887
Notes
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Reaction equation

HRID 1023887 reaction equation
CN(CC)C.C([O-])([O-])=O.[K+].[K+].[NH:12]1[CH2:16][CH2:15][CH2:14][C:13]1=[O:17].Br[C:19]1[CH:24]=[CH:23][C:22]([CH2:25][CH2:26][OH:27])=[CH:21][CH:20]=1>[Cu]I>[OH:27][CH2:26][CH2:25][C:22]1[CH:23]=[CH:24][C:19]([N:12]2[CH2:16][CH2:15][CH2:14][C:13]2=[O:17])=[CH:20][CH:21]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 11430Potassium CarbonateHCID 11723DimethylethylamineHCID 120252-PyrrolidoneHCID 728512-(4-Bromophenyl)ethanol

Product 1

HCID 214891281-(4-(2-Hydroxyethyl)phenyl)pyrrolidin-2-oneYield 37%

Reagents, catalysts & solvents 1

HCID 24350
Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
Catalyst

Conditions

Temperature
130 °C

Procedure

A mixture of CuI (0.198 mmol), N,N-dimethylethylamine (0.398 mmol), K2CO3 (3.98 mmol) and pyrrolidin-2-one (3.98 mmol) was purged with nitrogen gas. 2-(4-bromophenyl)ethanol (1.99 mmol) was added and the mixture was purged with purged again with nitrogen. The reaction mixture was stirred at 130° C. overnight. After cooling to room temperature, the reaction mixture was diluted with water (25 mL), NH4OH (5 mL) and the aqueous layer was extracted with dichloromethane (3×40 mL). The combined organic extracts were dried over sodium sulfate and evaporated under reduced pressure; the crude was purified by column chromatography to afford the final product. Yield=37%.

Workup

  1. customwas purged with nitrogen gas
  2. customthe mixture was purged
  3. customwith purged again with nitrogen
  4. temperatureAfter cooling to room temperature
  5. additionthe reaction mixture was diluted with water (25 mL), NH4OH (5 mL)
  6. extractionthe aqueous layer was extracted with dichloromethane (3×40 mL)
  7. dry with materialThe combined organic extracts were dried over sodium sulfate
  8. customevaporated under reduced pressure
  9. customthe crude was purified by column chromatography

Sources & evidence

ORD record
ord-cac7aea0fdfc45639101761658c312fb
Source dataset
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08722720B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes