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Sodium hydride → 3-(3-{4-[(6-Hydroxyhexyl)oxy]butyl}phenyl)imidazolidine-2,4-dione

HRID 857091
Notes
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Reaction equation

HRID 857091 reaction equation
C([O:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]1[CH:17]=[C:18]([NH:22][C:23]([NH:25][CH2:26][C:27]([O:29]CC)=O)=[O:24])[CH:19]=[CH:20][CH:21]=1)(=O)C.[H-].[Na+]>C(O)C>[OH:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]1[CH:17]=[C:18]([N:22]2[C:27](=[O:29])[CH2:26][NH:25][C:23]2=[O:24])[CH:19]=[CH:20][CH:21]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24758Sodium hydrideHCID 21867037Ethyl N-({[3-(4-{[6-(acetyloxy)hexyl]oxy}butyl)phenyl]amino}carbonyl)glycinate

Product 1

HCID 218671563-(3-{4-[(6-Hydroxyhexyl)oxy]butyl}phenyl)imidazolidine-2,4-dioneYield 112.7%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
75 °C

Procedure

A solution of ethyl N-({[3-(4-{[6-(acetyloxy)hexyl]oxy}butyl)phenyl]amino}-carbonyl)glycinate (2.967 g) in ethanol (30 ml) was treated under nitrogen with sodium hydride (60% oil dispersion; 280 mg) and the mixture was stirred for 18 h. The solvent was removed under reduced pressure, the residue was dissolved in acetic acid (10 ml) and conc. HBr (1 ml) and the mixture was heated to 75° C. for 1 h. The solvent was removed under reduced pressure, the residue was partitioned between EtOAc and brine. The organic solution was washed with brine, dried and evaporated to dryness. The residue was dissolved in MeOH (30 ml), SOCl2 (0.5 ml) was added, and the solution was stirred for 2 h. The solvent was removed under reduced pressure to give the title compound (2.67 g) ES+ve 349 (MH)+.

Workup

  1. customThe solvent was removed under reduced pressure
  2. dissolutionthe residue was dissolved in acetic acid (10 ml)
  3. customThe solvent was removed under reduced pressure
  4. customthe residue was partitioned between EtOAc and brine
  5. washThe organic solution was washed with brine
  6. customdried
  7. customevaporated to dryness
  8. dissolutionThe residue was dissolved in MeOH (30 ml)
  9. additionSOCl2 (0.5 ml) was added
  10. stirringthe solution was stirred for 2 h
  11. customThe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-7865f67f42b9442fa95e1467b8cc04d0
Source dataset
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07144908B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes