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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348984Generated: October 25, 2026

Hydrochloric Acid → Methyl 4-butyl-8-cyano-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate

https://huagongshe.com/reaction/348984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 8-bromo-4-butyl-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 21086218—
ReactantHCID 178418260HCID 178418260—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductMethyl 4-butyl-8-cyano-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 2108620266.7%

Reaction Conditions

Temperature175 °C

Reaction Steps

To a flask containing methyl 8-bromo-4-butyl-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate (0.33 g) was added NMP (7 mL), followed by copper cyanide (0.18 g). The mixture was then heated to 175° C. and stirred overnight. The resulting mixture was cooled to room temperature and poured into 1 N hydrochloric acid. The acidic aqueous layer was extracted with ethyl acetate, washed with 1 N hydrochloric acid (15 mL), saturated sodium bicarbonate (15 mL), and brine, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:9 ethyl acetate/hexanes) provided 184 mg of the title compound: 1H NMR (300 MHz, CDCl3) δ 7.55, 7.43, 4.41, 3.89, 3.39, 3.31, 1.58, 1.40, 0.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-36cb40f78eb54995aca347f0d29dc574
Source noteuspto-grants-2007_02