N,N-Dimethylaniline → HCID 19077574, compound

HRID 964607Notes

Reaction equation

HRID 964607 reaction equation
[Cl:1]C(Cl)(Cl)C(Cl)=O.[CH3:8][O:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14]O)=[CH:12][CH:11]=1.CN(C)C1C=CC=CC=1.[NH:27]1[CH2:32][CH2:31][CH2:30][CH:29]([C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH2:28]1.C(=O)([O-])[O-].[K+].[K+]>C1(C)C=CC=CC=1.ClCCl.CCCCCC.C(OCC)(=O)C>[ClH:1].[CH3:8][O:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14][N:27]2[CH2:32][CH2:31][CH2:30][CH:29]([C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH2:28]2)=[CH:12][CH:11]=1

Participants

10

Procedure

A solution of trichloroacetyl chloride (11.1 ml, 99 mmol) in toluene (30 ml) was added dropwise over 45 minutes to a stirred, ice-cooled solution of 4-methoxybenzyl alcohol (12.4 ml, 99 mmol) and N,N-dimethylaniline (12.6 ml, 99 mmol) in toluene (100 ml). The cooling bath was removed and stirring continued at room temperature for 1.5 hours, then the reaction mixture was filtered to remove the N,N-dimethylaniline hydrochloride which was washed with toluene (30 ml). A stirred mixture of the combined filtrate and washings, ethyl 3-piperidinecarboxylate (14.0 ml, 90 mmol) and anhydrous potassium carbonate (13.7 g, 99 mmol), under nitrogen, was heated under reflux for 110 hours, allowed to cool and filtered. Evaporation of the filtrate under reduced pressure gave a brown oil which was dissolved in dichloromethane (100 ml) and the resulting solution washed successively with 2M aqueous sodium carbonate solution (100 ml) and ca. 5M hydrochloric acid (200 ml), dried (Na2SO4) and evaporated under reduced pressure to provide a viscous oil. This oil was stirred at room temperature with a 1:1 mixture of ethyl acetate:hexane (100 ml) to produce a solid which was purified by successive trituration with the same solvent mixture (4×50 ml) to afford the title compound (6.11 g). Rf 0.85 (SS 1). Found: C,59.41; H,7.50; N,4.15. C16H23NO3 ; HCl; 0.50 H2O requires C,59.52; H,7.80; N,4.34%

Workup

  1. customThe cooling bath was removed
  2. filtrationthe reaction mixture was filtered
  3. customto remove the N,N-dimethylaniline hydrochloride which
  4. washwas washed with toluene (30 ml)
  5. temperatureunder nitrogen, was heated
  6. temperatureunder reflux for 110 hours
  7. temperatureto cool
  8. filtrationfiltered
  9. customEvaporation of the filtrate under reduced pressure
  10. customgave a brown oil which
  11. washthe resulting solution washed successively with 2M aqueous sodium carbonate solution (100 ml) and ca. 5M hydrochloric acid (200 ml)
  12. dry with materialdried (Na2SO4)
  13. customevaporated under reduced pressure
  14. customto provide a viscous oil
  15. customwas purified by successive trituration with the same solvent mixture (4×50 ml)

Sources & evidence

ORD record
ord-3a3f5f2515594bd396ff59c394984ec1
Source dataset
uspto-grants-1998_06
Patent number
US05770611

Reaction notes

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