HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-Chloro-furo[3,4-c]quinolin-1(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Chloro-furo[3,4-c]quinoline-1,3-dione | HCID 54104238 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Chloro-furo[3,4-c]quinolin-1(3H)-one | HCID 11206766 | — |
| Product | HCID 57030353 | HCID 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-Chloro-furo[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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05243049 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-fdab9219ef3743deb64f5cb01f5301ba |
| Source note | uspto-grants-1993_09 |