Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 53962231 | HCID 53962231 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 3063369 | HCID 3063369 | 96% |
Reaction Steps
To 2-[2-(3-thienyl)vinyl]-4H-3,1-benzoxazine-4-one (800 mg, 3.13 mmol) was added 1N-NaOH (21.9 ml) and the mixture was heated to 70° C. After adding methanol (30 ml), and the mixture was reacted for 1 hour. The methanol was removed from the reaction mixture under reduced pressure, and the residue was acidified with 10% HCl under cooling (pH about 4) to give a white solid, which was collected on a filter, washed with water, and dried to give the title compound (826 mg, yield, 96%). m.p., 218°-219° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05006548 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-69e87baa4b3d41e19c0442f88be181e0 |
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| Source note | uspto-grants-1991_04 |
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