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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44249Generated: October 25, 2026

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

https://huagongshe.com/reaction/44249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMorpholineHCID 8083—
Reactant1-Methyl-1H-pyrrole-2-carbaldehydeHCID 14504—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product1-methyl-4-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehydeHCID 86650822—
Product1-methyl-5-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehydeHCID 86650823—

Reaction Conditions

Temperature50 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541412B2
Source datasetuspto-grants-2013_09
ORD IDord-8838bff23f08415f88fe29d9cdc72eae
Source noteuspto-grants-2013_09