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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
Reactant4-chloro-5H,6H,7H-cyclopenta[b]pyridineHCID 12203327—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
Product4-Methoxy-6,7-dihydro-5H-cyclopenta[b]pyridineHCID 8672668344%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-c9c30d8c57d94708b00078f53a59c81f
Source noteuspto-grants-2015_12