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HRID 433878Erstellt: 25. Oktober 2026

Water → Methyl 3-formyl-4,5-dimethyl-1-[(1S,2S)-2-methylcyclopropylmethyl]pyrrole-2-carboxylate

https://huagongshe.com/reaction/433878

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl 3-formyl-4,5-dimethyl-1H-pyrrole-2-carboxylateHCID 10773740—
Edukt(1S,2S)-1-(bromomethyl)-2-methylcyclopropaneHCID 12110454—
EduktPotassium tert-butoxideHCID 23665647—
Katalysator18-Crown-6HCID 28557—
Katalysator(1S,2S)-1-(bromomethyl)-2-methylcyclopropaneHCID 12110454—
KatalysatorPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 3-formyl-4,5-dimethyl-1-[(1S,2S)-2-methylcyclopropylmethyl]pyrrole-2-carboxylateHCID 12110455103,9%

Reaktionsschritte

Potassium tert-butoxide (3.94 g, 35.1 mmol) was added to a solution of methyl 3-formyl-4,5-dimethylpyrrole-2-carboxylate (5.79 g, 31.9 mmol) and 18-crown-6 (0.41 g, 1.55 mmol) in tetrahydrofuran (130 ml) and the mixture was stirred at room temperature for 1 hour. After dropwise addition over 30 minutes of (1S,2S)-2-methylcyclopropylmethyl bromide (5.71 g, 38.3 mmol) to the reaction mixture at 50° C., the mixture was heated under reflux for 3 hours. Potassium tert-butoxide (0.36 g, 3.22 mmol) and (1S,2S)-2-methylcyclopropylmethyl bromide (0.48 g, 3.21 mmol) was further added to the mixture and this mixture was heated for 1 hour. The reaction mixture was poured into iced water and extracted with ethyl acetate. The extract was washed with water and saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The solvent was removed in vacuo to afford the desired compound (8.26 g, 100%) as a pale brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06670360B2
Quelldatensatzuspto-grants-2003_12
ORD IDord-0dc97801e5514eb9a8955208a882fd3e
Quellennotizuspto-grants-2003_12