HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 58087146, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1H-Pyrrolo(2,3-b)pyridine | HCID 9222 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-[(4-Chlorophenyl)methoxy]-3-methoxybenzaldehyde | HCID 718263 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58087146 | HCID 58087146 | 74% |
Reaction Steps
To 1H-Pyrrolo[2,3-b]pyridine (6, 0.235 g, 1.99 mmol) and 4-(4-chlorobenzyloxy)-3-methoxybenzaldehyde (23, 0.500 g, 1.81 mmol) was added 5 mL of methanol followed by the addition of solid potassium hydroxide (0.203 g, 3.61 mmol). The reaction was allowed to stir at ambient temperature for 18 days. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was separated and volatiles removed to give a solid which was suspended in hot ethyl acetate. The suspension was allowed to cool and the solid collected by vacuum filtration to provide 24 (548 mg, 74%). MS (ESI) [M+H+]+=409.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872018B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-12f547ca545148acb8fc9ecd495e3dae |
| Source note | uspto-grants-2011_01 |