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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55811Generated: October 29, 2026

Ethyl 4-(3-chloro-6-methoxyquinolin-2-yl)cyclohex-3-enecarboxylate → Ethyl 4-(3-chloro-6-methoxyquinolin-2-yl)cyclohexanecarboxylate

https://huagongshe.com/reaction/55811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-(3-chloro-6-methoxyquinolin-2-yl)cyclohex-3-enecarboxylateHCID 66980116—
SolventEthanolHCID 702—
ProductEthyl 4-(3-chloro-6-methoxyquinolin-2-yl)cyclohexanecarboxylateHCID 6698004326%

Reaction Conditions

Temperature30 °C

Reaction Steps

To ethyl 4-(3-chloro-6-methoxyquinolin-2-yl)cyclohex-3-enecarboxylate (900 mg, 2.60 mmol) in EtOH (40 mL) was added Rh(PPh3)3Cl (90.0 mg 0.0900 mmol). The mixture was stirred at 30° C. for 4 days under H2 (15 psi). The mixture was filtered off and the filtrate was concentrated to give the crude product, which was purified by silica gel column (PE/EtOAc=10/1) to give the desired product (234 mg, yield 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09433618B2
Source datasetuspto-grants-2016_09
ORD IDord-bc2979324f80478fb69e170f3d062b96
Source noteuspto-grants-2016_09