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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253114Generated: October 30, 2026

ethyl quinoline-3-carboxylate → Ethyl 1,2,3,4-tetrahydroquinoline-3-carboxylate

https://huagongshe.com/reaction/253114

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl quinoline-3-carboxylateHCID 282842—
SolventAcetic AcidHCID 176—
ProductEthyl 1,2,3,4-tetrahydroquinoline-3-carboxylateHCID 1241575998.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

Borane-pyridine complex (8 M, 292 mL, 2.34 mmol) was added to a solution of Ethyl quinoline-3-carboxylate (235 mg, 1.17 mmol) in acetic acid (10 mL). The solution was stirred at 25° C. for 20 h. The reaction mixture was concentrated in vacuo, basified with 1 M sodium carbonate (30 mL), and the product was extracted with dichloromethane (3×35 mL). The organic layers were dried over sodium sulfate and concentrated. Purification of the product by flash column chromatography (10% to 20% EtOAc/hexane) afforded the title compound (239 mg, 1.15 mmol). MS m/z: 206 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872009B2
Source datasetuspto-grants-2011_01
ORD IDord-fe50d86f25214fa491b2f1f3f992f04c
Source noteuspto-grants-2011_01