Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Indole-4-carboxaldehyde | HCID 333703 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22139317 | HCID 22139317 | — |
Reaction Steps
Morpholine (0.24 ml, 2.7 mmol) and formaldehyde (37% aq; 0.21 ml, 2.7 mmol) were added to glacial acetic acid (3 ml) at 0° C. After stirring for 15 minutes 4-indolcarboxaldehyde (0.27 g, 1.9 mmol) was added. The mixture was stirred 5 minutes at 0° C. and then 3½h at room temperature, prior to the addition of water (6 ml) and washing with ether. The aqueous layer was made alkaline with 2N NaOH and then extracted with dichloromethane. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulfate and evaporated to afford 0.46 g of the entitled product as an oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07049312B1 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-16eb1a25a4974f5f99a9805fc8fd024c |
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| Source note | uspto-grants-2006_05 |
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