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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712907Generated: October 26, 2026

Hydrochloric Acid → 3-Cyclohexyl-7-hydroxy-3,4-dihydro-benzo[e][1,3]oxazin-2-one

https://huagongshe.com/reaction/1712907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantPyridinium hydrochlorideHCID 21584435—
Reactant3-Cyclohexyl-7-methoxy-3,4-dihydro-benzo[e][1,3]oxazin-2-oneHCID 67525490—
SolventWaterHCID 962—
Product3-Cyclohexyl-7-hydroxy-3,4-dihydro-benzo[e][1,3]oxazin-2-oneHCID 11849106—

Reaction Conditions

Temperature220 °C

Reaction Steps

A mixture of 66 g of 3-cyclohexyl-7-methoxy-3,4-dihydro-benzo[e][1,3]oxazin-2-one and 200 g of pyridinium HCl are heated without solvent on a metal bath to 220° C. for 45 minutes whilst stirring. Evolving HCl gas is sucked off. The mixture obtained is cooled to RT, the melt obtained is dissolved in H2O and EtOAc and two phases obtained are separated. The aqueous layer obtained is extracted with EtOAc and washed with 1N HCl, dried and concentrated in vacuo. The concentration residue obtained is filtered over silica gel and the filtration residue obtained is concentrated. 3-Cyclohexyl-7-hydroxy-3,4-dihydro-benzo[e][1,3]oxazin-2-one is obtained in crystallized form. m.p. 193-196°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795251B2
Source datasetuspto-grants-2010_09
ORD IDord-fd9135988db9472bb3dab424c45605a8
Source noteuspto-grants-2010_09