Triethylamine → HCID 18786983, Verbindung

HRID 1107380Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1107380
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:16]=[CH:15][CH:14]=[CH:13][C:9]=1[C:10]([OH:12])=O.Cl.[CH2:18]([O:20][C:21](=[O:25])[CH2:22][NH:23][CH3:24])[CH3:19].C1CCC(N=C=NC2CCCCC2)CC1.C1C=CC2N(O)N=NC=2C=1.CCN(CC)CC>C1COCC1>[CH2:18]([O:20][C:21](=[O:25])[CH2:22][N:23]([CH3:24])[C:10](=[O:12])[C:9]1[CH:13]=[CH:14][CH:15]=[CH:16][C:8]=1[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[CH3:1])[CH3:19]

Komponenten

7

Versuchsvorschrift

A mixture of 2-(methylphenyl)benzoic acid (3.09 g, 14.55 mmol), sarcosine ethyl ester hydrochloride salt (2.23 g, 14.55 mmol), DCC (3.0 g, 14.55 mmol), HOBT (1.97 g, 14.55 mmol) and Et3N (1.47 g, 14.55 mmol) in THF (50 mL) were stirred at ambient temperature for 48 hours. The reaction was evaporated and the residue dissolved in EtOAc. The EtOAc solution was washed with HCl (10%), saturated NaHCO3 and brine, and dried (MgSO4). The EtOAc solution was filtered through a plug of silica gel follwoed by a second filtration through a plug of neutral alumina. Evaporation of the solution gave N-methyl-N-[2-(methylphenyl)benzoyl]glycine ethyl ester (4.5 g); LRMS (M+H)+ =312.2.

Aufarbeitung

  1. customThe reaction was evaporated
  2. dissolutionthe residue dissolved in EtOAc
  3. washThe EtOAc solution was washed with HCl (10%), saturated NaHCO3 and brine
  4. dry with materialdried (MgSO4)
  5. filtrationThe EtOAc solution was filtered through a plug of silica gel
  6. filtrationfollwoed by a second filtration through a plug of neutral alumina
  7. customEvaporation of the solution

Quellen und Nachweise

ORD-Eintrag
ord-48524b28e2ea471da652b0f89104bba1
Quelldatensatz
uspto-grants-2000_05
Patentnummer
US06060462

Notizen zur Reaktion

Wird geladen…