HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499439Generated: October 29, 2026
Methanol → 4-Methoxy-6,7-dihydro-5H-cyclopenta[b]pyridine
https://huagongshe.com/reaction/1499439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-chloro-5H,6H,7H-cyclopenta[b]pyridine | HCID 12203327 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Methoxy-6,7-dihydro-5H-cyclopenta[b]pyridine | HCID 86726683 | 44% |
Reaction Steps
A mixture of 4-chloro-6,7-dihydro-5H-cyclopenta[b]pyridine (2.8 g, 18 mmol), MeOH (20 mL) and sodium methoxide (3.0 g, 56 mmol) was sealed in a pressurized flask and heated at 110° C. for 18 h. The mixture was diluted with EtOAc and neutralized with HCl to pH=1. The organic solvent was removed under reduced pressure. The resulting mixture was washed with ether twice, and then neutralized with Na2CO3 solution. The aqueous layer was extracted twice with EtOAc. The combined organic layers were dried, filtered and concentrated under reduced pressure to give the sub-title compound (1.20 g, 44%). LCMS calc. for C9H12NO (M+H)+: m/z=150.1. Found: 150.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200004B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-c9c30d8c57d94708b00078f53a59c81f |
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| Source note | uspto-grants-2015_12 |
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