METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE
METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE Basic information
- Product Name:
- METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE
- Synonyms:
-
- METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE
- BUTTPARK 96\50-36
- Methyl 4-formyl-1-methyl-1h-pyrrole-2-carboxylate, 95+%
- 4-Formyl-2-methoxycarbonyl-N-methylpyrrole
- 4-formyl-1-methyl-1H-Pyrrole-2-carboxylic acid methyl ester
- methyl 4-formyl-1-methyl-1H-pyrrole-2-carboxylate 98%
- Methyl 4-Formyl-1-methylpyrrole-2-carboxylate
- 1H-Pyrrole-2-carboxylic acid, 4-formyl-1-methyl-, methyl ester
- CAS:
- 67858-47-3
- MF:
- C8H9NO3
- MW:
- 167.16
- Mol File:
- 67858-47-3.mol
METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE Chemical Properties
- 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
METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE Usage And Synthesis
Synthesis
37619-24-2
4885-02-3
67858-47-3
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
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METHYL 4-FORMYL-1-METHYL-1H-PYRROLE-2-CARBOXYLATE(67858-47-3)Related Product Information
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