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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500452Generated: October 25, 2026

Sodium borohydride → 2-Cyclopentyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/500452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-CyclopentylquinolineHCID 21826432—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
Product2-Cyclopentyl-1,2,3,4-tetrahydroquinolineHCID 6504182892.1%

Reaction Steps

To a solution of 2-cyclopentylquinoline (7.95 g, 40.3 mmol) and nickel (II) chloride hexahydrate (1.63 g, 6.85 mmol) in methanol (120 ml) cooled in an ice/methanol bath was added sodium borohydride (6.1 g, 161.2 mmol) portionwise over 1.5 h. The cooling bath was removed and the reaction stirred for a further 30 minutes. The methanol was then removed in vacuo. To the resulting black precipitate was added 2 M hydrochloric acid (100 ml) and then basified with 10 M potassium hydroxide. The mixture was poured into a separating funnel and extracted with ether (4×200 ml). The combined organic layers were dried (MgSO4), filtered and the solvent removed in vacuo to give 2-cyclopentyl-1,2,3,4-tetrahydroquinoline (7.45 g, 37.1 mmol) as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772227B2
Source datasetuspto-grants-2010_08
ORD IDord-3f234ec8a24c428ebc70d0e2e9896d2f
Source noteuspto-grants-2010_08