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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 1-Methyl-1H-pyrrole-2-carbaldehyde | HCID 14504 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-methyl-4-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehyde | HCID 86650822 | — |
| Product | 1-methyl-5-morpholin-4-ylmethyl-1H-pyrrole-2-carbaldehyde | HCID 86650823 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541412B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-8838bff23f08415f88fe29d9cdc72eae |
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| Source note | uspto-grants-2013_09 |
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