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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677331Generated: October 28, 2026

Hydrochloric Acid → 1-(7-Methoxy-4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-ethanone

https://huagongshe.com/reaction/1677331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-methyl-7-methoxy-3,4-dihydro-2H-[1,4]benzoxazineHCID 13671264—
Solvent1,2-DichloroethaneHCID 11—
Product1-(7-Methoxy-4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-ethanoneHCID 595985547.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

7-Methoxy-4-methyl-3,4-dihydro-2H-benzo[1,4]oxazine (11.17 g, 0.625 mol) in 400 mL of 1,2-dichloroethane was stirred at 0° C. under nitrogen. Aluminum trichloride (8.3 g, 0.625 mol) was added in portions, followed by dropwise addition of acetyl chloride (4.9 mL, 0.678 mol). The reaction mixture was stirred at 0° C. for 2.5 hours. Aluminum trichloride (3 g) was added, and the reaction mixture was stirred at room temperature for 24 hours. The reaction mixture was poured into ice and 550 mL 3N HCl was added. The aqueous mixture was extracted with methylene chloride, and the combined organic layers were dried (MgSO4), filtered, and evaporated under reduced pressure to yield 10.48 g of 1-(7-Methoxy-4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-ethanone. (M+H)=222.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008313B2
Source datasetuspto-grants-2011_08
ORD IDord-2974be2a19c84084ac6c5fc292b6312f
Source noteuspto-grants-2011_08