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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696300Generated: October 26, 2026

Acetyl chloride → ethyl 4-acetyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate

https://huagongshe.com/reaction/1696300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantEthyl 3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 31090—
ReactantDiisopropylethylamineHCID 81531—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Productethyl 4-acetyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylateHCID 1342508366.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

Acetyl chloride (23 L, 0.33 mmol) was added to a solution of (±)-ethyl 3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylate (Example 3a, 55 mg, 0.27 mmol), DMAP (1.6 mg, 0.013 mmol), and Hunig's base (63 L, 0.36 mmol) in dichloromethane (2 mL). The solution was stirred at 25° C. for 24 h, then the reaction mixture was diluted with dichloromethane (60 mL) and the mixture was extracted with 0.1 M sodium carbonate (7 mL) and half-saturated brine (7 mL). The organic layer was dried over sodium sulfate and concentrated. Purification of the product by flash column chromatography (40% EtOAc/hexane) afforded the title compound (46 mg, 0.18 mmol). MS m/z: 250 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163766B2
Source datasetuspto-grants-2012_04
ORD IDord-d9b93c1dee6f47228a481e2b53d3e33d
Source noteuspto-grants-2012_04