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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348983Generated: October 25, 2026

Chloroacetyl chloride → Methyl 8-bromo-4-butyl-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate

https://huagongshe.com/reaction/348983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3-bromo-5-(butylamino)-4-hydroxybenzoateHCID 21086159—
ReactantIsobutyl methyl ketone waterHCID 22737866—
SolventChloroformHCID 6212—
ProductMethyl 8-bromo-4-butyl-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 21086218—

Reaction Steps

To an ice-cold, stirred solution of Methyl 3-bromo-5-(butylamino)-4-hydroxybenzoate (440 mg) and sodium bicarbonate (280 mg) in 1:1 isobutyl methyl ketone/water (10 mL) was added chloroacetyl chloride (226 mg). The mixture was stirred for 1 h, warmed to room temperature, and heated at reflux for 14 h. The mixture was cooled to room temperature, diluted with chloroform, and the layer separated. The organic layer was washed with water, and brine, dried (magnesium sulfate), filtered, and concentrated under reduced pressure to give a white solid: 1H NMR (300 MHz, CDCl3) δ 7.94, 7.62, 4.76, 3.98, 3.93, 1.65, 1.43, 0.97, which was used in the next step without further purification or characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-5ebcb16739f74f90aa96197bb81c0e20
Source noteuspto-grants-2007_02