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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015425Generated: November 1, 2026

Ammonium Chloride → HCID 67300903, compound

https://huagongshe.com/reaction/1015425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67301095HCID 67301095—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67300903HCID 6730090340.1%

Reaction Steps

To a solution of 5-[5-(naphthalen-1-yloxy)-pentyloxy]-quinoline (0.83 g, 2.32 mmol) in 10 mL methanol and 1 mL THF was added sodium borohydride (0.35 g, 9.29 mmol) and nickel (II) chloride hexahydrate (0.28 g, 1.16 mmol). The reaction mixture was stirred overnight at room temperature and then 20 mL saturated aqueous ammonium chloride solution was added. The solution was extracted with ethyl acetate (3×20 mL), and the combined organic phases were washed with brine, dried over MgSO4, and concentrated to give a white solid. The crude product was purified by silica gel chromatography to give 5-[5-(naphthalen-1-yloxy)-pentyloxy]-1,2,3,4-tetrahydro-quinoline (335 mg, 0.93 mmol, 40%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985763B2
Source datasetuspto-grants-2011_07
ORD IDord-141413edab5a4c11822710c84cc26728
Source noteuspto-grants-2011_07