HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698341Generated: October 27, 2026
Ammonium Chloride → 6-amino-4-(3-methoxy-propyl)-2,2-dimethyl-4H-benzo[1,4]oxazin-3-one
https://huagongshe.com/reaction/1698341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(3-methoxy-propyl)-2,2-dimethyl-6-nitro-4H-benzo[1,4]oxazin-3-one | HCID 57790722 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-amino-4-(3-methoxy-propyl)-2,2-dimethyl-4H-benzo[1,4]oxazin-3-one | HCID 57791174 | 105.2% |
Reaction Steps
At room temperature, an ethanolic solution (80 ml) of 4-(3-methoxy-propyl)-2,2-dimethyl-6-nitro-4H-benzo[1,4]oxazin-3-one (9.76 g, 33.2 mmol) is treated with H2O (80 ml), NH4Cl (3.58 g, 66.9 mmol), and powdered Zn (10.97 g, 0.17 mol), heated to 80° C., stirred for 2 h under reflux, cooled to room temperature, and filtered via celite pad. After washing the cake with CH2Cl2 for several times, the both layers of the combined filtrate are separated. The aq. layer is treated with 5N NaOH (6.0 ml) to adjust its pH 9˜10, and extracted with CH2Cl2 (3×100 ml). The combined org. layer is washed with sat. aqueous solution of NaHCO3 (100 ml) and brine (50 ml), dried (Na2SO4), and evaporated. A SiO2 flash chromatography (250 g, CH2Cl2/acetone 3:1) gives 6-amino-4-(3-methoxy-propyl)-2,2-dimethyl-4H-benzo[1,4]oxazin-3-one (9.23 g, 99%) as brown oil. Rf(CH2Cl2/EtOAc 2:1) 0.34. 1H-NMR (400 MHz, CDCl3) 1.39 (s), 1.80-1.91 (m, 2 H), 3.28 (s), 3.35 (t, J=8.0), 3.44 (br. s), 3.88 (t, J=9.0), 6.23 (dd, J=9.0, 0.4), 6.33 (d, J=0.4), 6.68 (d, J=9.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163773B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-acb0e62b175c4932a68edb0622d7560e |
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| Source note | uspto-grants-2012_04 |
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