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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266159Generated: November 2, 2026

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

https://huagongshe.com/reaction/2266159

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 pourd 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 numberUS07858632B2
Source datasetuspto-grants-2010_12
ORD IDord-257e218275234c99be2be51f7bd70f4a
Source noteuspto-grants-2010_12