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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896146Generated: October 29, 2026

Dichloromethane → 7-amino-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-3-one

https://huagongshe.com/reaction/896146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAmmonium ChlorideHCID 25517—
Reactant2H-1,4-Benzoxazin-3(4H)-one, 4-methyl-7-nitro-HCID 21877805—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product7-amino-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 2764460—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred suspension of 4-methyl-7-nitro-2H-1,4-benzoxazin-3-one (DE 19802239, 2.43 g, 11.67 mmol) in EtOH (20 mL) and water (10 mL) is added ammonium chloride (6.25 g, 116.70 mmol). To this mixture is added iron (1.95 g, 35.00 mmol) in 3 equal portions. The resulting mixture is heated to 80° C. for 2 h at which time the reaction is cooled to room temperature followed by addition of CH2Cl2 (100 mL). The resulting mixture is filtered through celite and the filtrate is further diluted with water (100 mL). The organic layer is separated followed by further extraction of the aqueous phase with CH2Cl2 (3×50 mL). The organic phases are combined, dried over Na2SO4 and concentrated under reduced pressure, and the product is purified by silica gel column chromatography (EtOAc) to give the title compound in quantitative yield, MS m/z 179.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919329B2
Source datasetuspto-grants-2005_07
ORD IDord-87a17b8d403f4975805c57249d8aae28
Source noteuspto-grants-2005_07