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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727818Generated: November 1, 2026

Tetrahydrofuran → HCID 10766034, compound

https://huagongshe.com/reaction/727818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 131716996HCID 131716996—
SolventDiethyl EtherHCID 3283—
ProductHCID 10766034HCID 10766034—

Reaction Steps

To a solution of 8-chloro-2,2-dibutyl-3,4-dihydro-(5(2-quinolylmethoxy)-1(2H)-naphthalenone (180 mg) in freshly distilled tetrahydrofuran (5 ml) was added lithium aluminum hydride (15 mg) with stirring in an ice bath under nitrogen and the mixture was stirred for minutes in an ice bath. To the mixture was carefully added aqueous saturated ammonium chloride solution (5 ml) in an ice bath, and then diethylether (10 ml) was added thereto. The separated aqueous layer was extracted two times with diethyl ether and the combined organic layers were washed with brine. The organic layer was dried over magnesium sulfate and concentrated in vacuo to give the oily residue which was crystallized from diisopropyl ether to yield 8-chloro-2,2-dibutyl-5-(2-quinolylmethoxy)-1,2,3,4-tetrahydro-1-naphthol (142 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045548
Source datasetuspto-grants-1991_09
ORD IDord-4b529074a2d64b69bca12c576fb201e1
Source noteuspto-grants-1991_09