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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium NitriteHCID 23668193—
Reactant6-Iodo-4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazineHCID 68162103—
SolventAcetic AcidHCID 176—
Product4-methyl-3,4-dihydro-2H-1,4-benzoxazin-6-amineHCID 22598422—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328114B2
Source datasetuspto-grants-2016_05
ORD IDord-8d22183bef8244088ce4f2160d19a6e5
Source noteuspto-grants-2016_05