HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551809Generated: October 30, 2026
Methyl 3-amino-4-hydroxybenzoate → methyl 3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate
https://huagongshe.com/reaction/551809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3-amino-4-hydroxybenzoate | HCID 10815 | — |
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate | HCID 16244461 | — |
Reaction Steps
5.16 g of methyl 3-amino-4-hydroxybenzoate are dissolved in 100 ml of dimethylformamide in a 500 ml round-bottomed flask. 17.06 g of potassium carbonate and then 7.98 ml of dibromoethane are subsequently added. The reaction medium is heated at 110° C. with stirring for five hours. After evaporating the solvent, water and ethyl acetate are added. The aqueous phase is extracted three times with ethyl acetate. The organic phases are combined and then dried over magnesium sulfate and the solvent is evaporated under reduced pressure. The residue is chromatographed on silica gel with a heptane/ethyl acetate 6/4 mixture. 3.61 g of methyl 3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07947834B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-1b5cdb75d3d14604ac5d296ed2596db0 |
|---|
| Source note | uspto-grants-2011_05 |
|---|