HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970318Generated: October 25, 2026
1,1-Dibromoethane → 2H-1,4-Benzoxazine, 3,4-dihydro-4-methyl-
https://huagongshe.com/reaction/970318
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | o-(Methylamino)phenol | HCID 69138 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2H-1,4-Benzoxazine, 3,4-dihydro-4-methyl- | HCID 3755024 | 79% |
Reaction Steps
To a mixture of 104A (2.33 g, 18.9 mmol) and dibromoethane (6.5 mL, 75.7 mmol) in a mixture of acetone (80 mL) and water (20 mL) at room temperature was added potassium carbonate (10.46 g, 75.7 mmol). The mixture was heated at reflux for 3 days. HPLC indicated that the reaction was complete, and the acetone was removed under reduced pressure. The aqueous residue was extracted with DCM, washed with water, and dried over anhydrous sodium sulfate. Concentration under reduced pressure followed by purification by silica gel chromatography afforded 104B (2.22 g, 79%). HPLC retention time=2.07 min. (Condition B) and LC/MS M+1=150.08. 1H-NMR (500 MHz, CDCl3) δ 2.91 (s, 3H), 3.28 (t, 2H), 4.33 (t, 2H), 6.70 (t, 1H, J=7.5 Hz), 6.72 (d, 1H, J=7.5 Hz), 6.82 (d, 1H, J=7.5 Hz), and 6.89 (t, 1H, J=7.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312209B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-95b64d6cec094887a8203eb207abaaa8 |
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| Source note | uspto-grants-2007_12 |
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