HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 6,7-Diacetoxy-4-chloro-quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 136013901 | HCID 136013901 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6,7-Diacetoxy-4-chloro-quinazoline | HCID 27281377 | — |
Reaction Steps
To a solution of 6,7-diacetoxy-4(3H)-quinazolinone, 12 (3.20 g, 11.42 mmol) in CHCl3 (60 ml) was added oxalyl chloride (2.2 ml, 17.3 mmol) dropwise at 0° C. The resulting reaction mixture was stirred at room temperature for 15 minutes then was gradually heated to reflux for 5 h during which time the starting material was consumed. The reaction mixture was cooled to 10° C. and the solution was quenched with aq sodium bicarbonate. The organic layer was separated and washed with brine then dried over Na2SO4 and directly taken to the next step without concentration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08343950B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-96315d7273964b919b307acc3bd5e19a |
| Source note | uspto-grants-2013_01 |