HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Acemetacin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Allyl 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-3-indoleacetoxyacetate | HCID 13654465 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acemetacin | HCID 1981 | — |
Reaction Steps
0.003 mole of tetrakis-triphenylphosphine-palladium-(O) is added to 0.03 mole of acemetacin allyl ester in 50 ml of tetrahydrofuran, under nitrogen. 0.3 mole of piperidine is added dropwise at 20°-25° C., with stirring, and stirring is then continued for 2 hours at room temperature (check by thin layer chromatography). 200 ml of half-concentrated hydrochloric acid are added dropwise with cooling, the phases are separated off, the aqueous phase is extracted twice with methylene chloride and the combined organic phases are evaporated in vacuo. The residue is recrystallised from toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04658039 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-f58d4d42e84347c99776474a7ff89b38 |
| Source note | uspto-grants-1987_04 |