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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Pyridinium hydrochloride | HCID 21584435 | — |
| Reactant | 3-Cyclohexyl-7-methoxy-3,4-dihydro-benzo[e][1,3]oxazin-2-one | HCID 67525490 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Cyclohexyl-7-hydroxy-3,4-dihydro-benzo[e][1,3]oxazin-2-one | HCID 11849106 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795251B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-fd9135988db9472bb3dab424c45605a8 |
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| Source note | uspto-grants-2010_09 |
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