HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13093538, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-(2-Chloro-6-methoxyphenyl)-1,3-oxazolidine-2,4-dione | HCID 13092015 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13093538 | HCID 13093538 | — |
Reaction Steps
5-(2-Chloro-6-methoxyphenyl)oxazolidin-2,4-dione (1.21 g., 5 mmoles) was dissolved in 10 ml. of tetrahydrofuran. Acetic anhydride (613 mg. 0.57 ml. 6 mmoles) was added and the solution stirred at room temperature for 44 hours. The reaction mixture was concentrated to an oil, partitioned between chloroform and saturated sodium bicarbonate. The chloroform layer was washed with fresh bicarbonate and then brine, dried over anhydrous magnesium sulfate, filtered, and concentrated to solid. Repulp of the residue in about 50 ml. of ether gave 3-acetyl-5-(2-chloro-6-methoxyphenyl)oxazolidin-2,4-dione (790 mg., 56%; m.p. 132°-135° C. m/e 285/283).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367234 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-cf61406a8411463ab5ecd2fdfe6627c8 |
| Source note | uspto-grants-1983_01 |