HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521596Generated: November 1, 2026
Sodium Nitrite → 4-methyl-3,4-dihydro-2H-1,4-benzoxazin-6-amine
https://huagongshe.com/reaction/521596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 6-Iodo-4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazine | HCID 68162103 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-methyl-3,4-dihydro-2H-1,4-benzoxazin-6-amine | HCID 22598422 | — |
Reaction Steps
6-Iodo-4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazine [S12-5]. To solution of S12-4 (2.1 g, 12.8 mmol) in 50 mL of acetic acid cooled in ice bath was added NaNO2 (1.77 g, 26.9 mmol) slowly in portions. The resulting mixture was stirred at 0° C. for 10 min and was added KI (4.24 g, 38.4 mmol) in portions. The reaction mixture was stirred at 0° C. for 30 min, allowed to warm up to rt and stirred for 2 h. The resulting mixture was quenched with 100 mL of water, extracted with ethyl acetate (3×150 mL). The organic layer was combined, treated with Na2S2O3, washed with brine, dried over MgSO4 and purified by flash chromatography to give S12-5 (1.86 g, 53%) as a yellow solid. 1H NMR (CDCl3, 500 MHz) δ 6.64 (d, J=8.3 Hz, 1H), 6.56 (s, 1H), 6.48 (d, J=8.4 Hz, 1H), 4.25 (m, 2H), 3.24 (m, 2H), 2.85 (s, 3H); 13C NMR (CDCl3, 125 MHz) δ 138.1, 126.6, 120.5, 117.6, 111.9, 83.7, 64.8, 48.7, 36.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328114B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8d22183bef8244088ce4f2160d19a6e5 |
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| Source note | uspto-grants-2016_05 |
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