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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1093969Erstellt: 26. Oktober 2026

Formaldehyde → 1-methyl-4-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehyde

https://huagongshe.com/reaction/1093969

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktMorpholineHCID 8083—
Edukt1-Methyl-1H-pyrrole-2-carbaldehydeHCID 14504—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt1-methyl-4-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehydeHCID 86650822—
Produkt1-methyl-5-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehydeHCID 86650823—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of morpholine (130 mmoles) in acetic acid (60 ml) at 0° C. there are added 1-methyl-1H-pyrrole-2-carbaldehyde (110 mmoles) and formaldehyde (110 mmoles) 37% in water. The reaction mixture is stirred for 16 hours at 50° C. After evaporation to dryness, about 100 ml of 25% aqueous sodium hydroxide solution are added. After extraction with DCM, the organic phase is washed with water and with saturated aqueous NaCl solution, dried over sodium sulphate, filtered and evaporated to dryness. The residue is purified by flash chromatography on silica gel (SiO2; gradient AcOEt/MeOH) to yield the title products 1-methyl-4-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehyde and 1-methyl-5-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehyde in a ratio of 1/5.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08133889B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-9649336304ea44fb80132f3e1b54a189
Quellennotizuspto-grants-2012_03