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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415714Generated: November 2, 2026

Sodium borohydride → 4-Chloro-furo[3,4-c]quinolin-1(3H)-one

https://huagongshe.com/reaction/1415714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Chloro-furo[3,4-c]quinoline-1,3-dioneHCID 54104238—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-furo[3,4-c]quinolin-1(3H)-oneHCID 11206766—
ProductHCID 57030353HCID 57030353—

Reaction Steps

To a well stirred mixture of 4-Chloro-furo[3,4-c]quinoline-1,3-dione (1.9 g) in tetrahydrofuran (10 mL) was added sodium borohydride (400 mg) at 0° C. and stirring was continued for 2 h. The reaction was then quenched with excess 6N HCl and water, and concentrated in vacuo to afford 4-Chlorofuro[3,4-c]quinolin-3(1H)-one as a pink solid along with a small quantity of 4-Chloro-furo[3,4-c]quinolin-1(3H)-one which could be isolated by column chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05908932
Source datasetuspto-grants-1999_06
ORD IDord-be038762e9c746a188cbd73dc99f2c13
Source noteuspto-grants-1999_06