HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456355Generated: October 25, 2026
Dimethylformamide → 6-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione
https://huagongshe.com/reaction/456355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-2h-1,3-benzoxazine-2,4(3h)-dione | HCID 90359 | — |
| Reactant | 1,10-Dibromodecane | HCID 221483 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione | HCID 22251422 | 49.9% |
Reaction Steps
A slurry of 9.77 g of 6-chloro-2H-1,3-benzoxazine-2,4(3H)-dione (50 mmol) and 60 ml of DMF was treated with a solution of 1,10-dibromodecane (52.52 g, 0.175 mol) and DMF (60 ml) was added. Diisopropylethylamine (9.6 ml, 55 mmol) was added dropwise. A thermometer and condenser were attached, and the flask was placed in an oil bath. The reaction was heated to 60 C. for approximately 3 hrs, cooled to 47 C. and hexanes (150 ml) were added. The mixture was diluted with water (175 ml). The resulting solids were removed by filtration. The aqueous layer was washed with warm hexanes. The resulting solids were filtered from the hexane layer and recrystallized from warm hexanes to give 10.39 g of 6-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07186414B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-3eb9aa6ce62546f78904c2eb2703b578 |
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| Source note | uspto-grants-2007_03 |
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