HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3,6-dihydro-3,5-dimethyl-6-(4-ethoxyphenyl)-2H-1,2-oxazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-t-butoxycarbonyl-3,6-dihydro-3,5-dimethyl-6-(4-ethoxyphenyl)-2H-1,2-oxazine | HCID 18401539 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,6-dihydro-3,5-dimethyl-6-(4-ethoxyphenyl)-2H-1,2-oxazine hydrochloride | HCID 18401532 | — |
Reaction Steps
Acetyl chloride (30 ml) was added dropwise over 10 mins to a cooled solution of methanol (300 ml) The resulting solution of hydrogen chloride in methanol was added to a stirred solution of 2-t-butoxycarbonyl-3, 6-dihydro-3,5-dimethyl-6-(4-ethoxyphenyl)-2H-1, 2-oxazine (11.6 g, 34.8 mmol) in methanol (50 ml). After 4 h at room temperature the mixture was evaporated to a solid (8.35 g), triturated with diethyl ether and the solid filtered to give 3,6-dihydro-3,5-dimethyl-6-(4-ethoxyphenyl)-2H-1,2-oxazine hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06482824B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-6dc271ae0152468a8254b5287a65bc5e |
| Source note | uspto-grants-2002_11 |