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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74063Generated: October 25, 2026

Acetyl chloride → 1-(6-nitro-2H-benzo[b][1,4]oxazin-4(3H)-yl)ethanone

https://huagongshe.com/reaction/74063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantSodium BicarbonateHCID 516892—
Reactant6-nitro-3,4-dihydro-2H-1,4-benzoxazineHCID 7062225—
SolventDichloromethaneHCID 6344—
Product1-(6-nitro-2H-benzo[b][1,4]oxazin-4(3H)-yl)ethanoneHCID 5786471490%

Reaction Steps

Under vigorous stirring at room temperature, acetyl chloride (1.02 g, 13 mmol) was added dropwise to a mixture of 6-nitro-3,4-dihydro-2H-benzo[1,4]oxazine (1.8 g, 10 mmol) and NaHCO3 (7.14 g, 85 mmol) in CH2Cl2 (50 mL). After addition, the reaction was stirred for 1 h at this temperature. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was treated with Et2O:hexane (1:2, 50 mL) under stirring for 30 min and then filtered to give 4-acetyl-6-nitro-3,4-dihydro-2H-benzo[1,4]oxazine as a pale yellow solid (2 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829204B2
Source datasetuspto-grants-2014_09
ORD IDord-7ccda5df6a2047b99cc019ca9cb59536
Source noteuspto-grants-2014_09