Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Butenoic acid, 2-hydroxy-3-methyl-, ethyl ester | HCID 10855589 | — |
| Reactant | methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate | HCID 15766845 | — |
| Catalyst | Tributylamine | HCID 7622 | — |
| Product | Pentoxazone | HCID 11714234 | 54.5% |
Reaction Steps
Methyl N-(4-chloro-5-cyclopentyloxy-2-fluorophenyl)carbamate (2.87 g, 10 mmol), ethyl 2-hydroxy-3-methyl-3-butenoate (4.32 g, 30 mmol), ferric chloride (162 mg, 1.0 mmol) and tributylamine (92.7 mg, 0.5 mmol) were introduced into a flask (25 cc) equipped with a distillation unit, and the reaction was conducted at 200° C. for 3 hours. After completion of the reaction, the reaction solution was allowed to cool to 70 to 80° C., and a mixed solution consisting of methanol (5 mL) and 6N hydrochloric acid (0.25 mL) was added thereto and mixed homogeneously. Then, the reaction solution was left to stand at room temperature. The precipitated solid was collected by filtration, washed with a mixed solution consisting of methanol (8 mL) and 6N hydrochloric acid (0.8 mL) and then water (10 mL) and dried completely under reduced pressure to obtain 3-(4-chloro-5-cyclopentyloxy-2-fluorophenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione (1.93 g, yield 54.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06090946 |
|---|
| Source dataset | uspto-grants-2000_07 |
|---|
| ORD ID | ord-ab997b7e954d4dacbfb0abb4b4861f3f |
|---|
| Source note | uspto-grants-2000_07 |
|---|