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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644337Generated: October 31, 2026

Bromoacetyl bromide → 3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-carbonitrile

https://huagongshe.com/reaction/1644337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
Reactant3-Amino-4-hydroxybenzonitrileHCID 271258—
ReactantSodium BicarbonateHCID 516892—
SolventChloroformHCID 6212—
Product3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-carbonitrileHCID 10654813—

Reaction Conditions

Temperature0 °C

Reaction Steps

The title compound was prepared similarly to literature procedure (Caliendo, G; et. al.; Bioorg. Med. Chem. Lett., 2002, 10, 2663), but in one step. Commercially available 3-amino-4-hydroxybenzonitrile (2.5 g, 18.6 mmol) was dissolved in chloroform (300 mL) and saturated sodium bicarbonate (90 mL). The biphasic reaction mixture was cooled to 0° C. and bromoacetyl bromide (2.4 mL, 28 mmol) was added dropwise. The reaction was stirred overnight at room temperature. The layers were separated and the aqueous layer was filtered to yield the desired product as a tan solid, 2.3 g (69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124602B2
Source datasetuspto-grants-2012_02
ORD IDord-df9b4e274a4846b8816022368982a983
Source noteuspto-grants-2012_02