HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660779Generated: October 31, 2026
1,2-Dibromoethane → methyl 3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate
https://huagongshe.com/reaction/1660779
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Methyl 3-amino-4-hydroxybenzoate | HCID 10815 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate | HCID 16244461 | — |
Reaction Steps
A solution of 3-amino-4-hydroxy-benzoic acid methyl ester (4.2 g, 25.4 mmol) in dimethylformamide (85 mL) was treated with K2CO3 (14.2 g, 102.9 mmol, 4 equiv.) and 1,2-dibromoethane (19.3 g, 102.9 mmol, 4 equiv.). The mixture was stirred at 70° C. overnight, then filtered to remove the solids. The filtrate was removed under vacuo, and the residue was purified by flash chromatography (heptane/ethyl acetate gradient) to yield 3,4-dihydro-2H-benzo[1,4]oxazine-6-carboxylic acid methyl ester, 3.65 g (73%) as a light yellow solid, MS (ISP): m/e=235.1 (M+CH3CN+.); δH (300 MHz; CDCl3) 7.36 (1H, dd, J=8.5, 2.0), 7.30 (1H, d, J=2.0), 6.78 (1H, d, J=8.5), 4.30 (2H, m); 3.85 (3H, s), 3.43 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030308B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-66980f4e5e84451e9c5c214c0962986d |
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| Source note | uspto-grants-2011_10 |
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