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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(3-methoxy-propyl)-2,2-dimethyl-6-nitro-4H-benzo[1,4]oxazin-3-oneHCID 57790722—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Product6-amino-4-(3-methoxy-propyl)-2,2-dimethyl-4H-benzo[1,4]oxazin-3-oneHCID 57791174105.2%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163773B2
Source datasetuspto-grants-2012_04
ORD IDord-acb0e62b175c4932a68edb0622d7560e
Source noteuspto-grants-2012_04