HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520284Generated: October 29, 2026
Anthranilic Acid → 2-Ethyl-benzo[d][1,3]oxazin-4-one
https://huagongshe.com/reaction/520284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Anthranilic Acid | HCID 227 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Ethyl-benzo[d][1,3]oxazin-4-one | HCID 928526 | 78.2% |
Reaction Steps
Propanoyl chloride (6.2 g, 67 mmol) was added to a solution of anthranilic acid (1 g, 7.3 mmol) in dichloromethane (20 mL). The reaction medium was kept under reflux and agitation, with the end of the reaction being monitored by CG/MS. After the end of the reaction, a hydrochloric acid solution was added (20 mL, 1M), and the resulting mixture was extracted with ethyl acetate (100 mL), the extract was dried with magnesium sulfate and the solvent was evaporated. Acetic anhydride (15 mL) was added to the residue and the reaction medium was taken to reflux and accompanied through CG/MS in order to monitor cyclization. After the end of the reaction, the reaction medium spin dried at a temperature of 65° C. using portions of toluene to facilitate the elimination of the anhydride. 1.0 g of the raw product 2-ethyl-4H-3,1-benzoxazin-4-one was obtained, which was used directly in the stage subsequent to reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09326984B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-08f43ef456a94ac9b0bbabc66dc8ef5a |
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| Source note | uspto-grants-2016_05 |
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