Identification | Back Directory | [Name]
METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE | [CAS]
67858-47-3 | [Synonyms]
BUTTPARK 96\50-36 4-Formyl-2-methoxycarbonyl-N-methylpyrrole Methyl 4-Formyl-1-methylpyrrole-2-carboxylate METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE methyl 4-formyl-1-methyl-1H-pyrrole-2-carboxylate 98% Methyl 4-formyl-1-methyl-1h-pyrrole-2-carboxylate, 95+% 4-formyl-1-methyl-1H-Pyrrole-2-carboxylic acid methyl ester 1H-Pyrrole-2-carboxylic acid, 4-formyl-1-methyl-, methyl ester | [Molecular Formula]
C8H9NO3 | [MDL Number]
MFCD01571196 | [MOL File]
67858-47-3.mol | [Molecular Weight]
167.16 |
Chemical Properties | Back Directory | [Melting point ]
100 °C | [Boiling point ]
293.1±25.0 °C(Predicted) | [density ]
1.16±0.1 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
-9.84±0.70(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
AlCl3 (21.08 g, 158.1 mmol) was slowly added at -25 °C in a mixed solvent of 1,2-dichloroethane (100 mL) and nitromethane (100 mL) as methyl 1-methylpyrrole-2-carboxylate (10 g, 71.86 mmol) and 1,1-dichlorodimethyl ether (8.26 g, 71.86 mmol). The reaction mixture was stirred continuously at -25 °C for 0.5 hours. Upon completion of the reaction, the mixture was carefully poured into ice water (100 mL) to quench the reaction. Subsequently, the organic layer was separated by extraction with dichloromethane (100 mL) and water (100 mL). The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate/petroleum ether=1/1) to afford methyl 4-formyl-N-methylpyrrole-2-carboxylate (11.77 g, 70.42 mmol, 98% yield) as a yellow solid. Mass spectrum (EI+, m/z): 168.2 [M+H]+. NMR hydrogen spectrum (400 MHz, DMSO-d6) δ 9.71 (s, 1H), 7.91 (d, J=1.8 Hz, 1H), 7.22 (d, J=1.8 Hz, 1H), 3.92 (s, 3H), 3.78 (s, 3H).NOESY experiments further confirmed the structure of the target compound. | [References]
[1] Patent: WO2018/89493, 2018, A1. Location in patent: Paragraph 00215 [2] Medicinal Chemistry Research, 1995, vol. 5, # 6, p. 426 - 430 |
|
|