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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49935Generated: October 25, 2026

6-Quinolinecarboxylic acid, ethyl ester → Ethyl 1,2,3,4-tetrahydroquinoline-6-carboxylate

https://huagongshe.com/reaction/49935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Quinolinecarboxylic acid, ethyl esterHCID 94670—
ReactantSodium borohydrideHCID 4311764—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
ProductEthyl 1,2,3,4-tetrahydroquinoline-6-carboxylateHCID 13951736—

Reaction Steps

257 mg (1.1 mmol) of nickel chloride hexahydrate and then 770 mg (20.3 mmol) of sodium borohydride were added to a mixture of 1.00 g (5.0 mmol) of ethyl quinoline-6-carboxylate and 15 ml of methanol under cooling with ice, and they were stirred at room temperature for 20 minutes. Methanol was evaporated, and the residue was purified by the silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710056B2
Source datasetuspto-grants-2004_03
ORD IDord-4e6a8430b1e340cdad7e86ff4ab13562
Source noteuspto-grants-2004_03