HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-[4-(4-Chlorophenyl)-2-oxazolyl]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-[4-(4-chlorophenyl)-2-oxazolyl]benzoate | HCID 18613897 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[4-(4-Chlorophenyl)-2-oxazolyl]benzoic acid | HCID 12070662 | 64% |
Reaction Steps
A mixture of methyl 4-[4-(4-chlorophenyl)-2-oxazolyl]benzoate (450 mg), a 1N aqueous solution of sodium hydroxide (2.5 ml), tetrahydrofuran (10 ml) and methanol (5 ml) was stirred at 60 to 70° C. for 20 minutes. The reaction mixture was poured into water. To the mixture was added 1N hydrochloric acid, and precipitated 4-[4-(4-chlorophenyl)-2-oxazolyl]benzoic acid (273 mg, Yield: 64%) was collected by filtration and then washed with water. The product was recrystallized from acetone-isopropyl ether to obtain pale yellow prisms. Melting Point: 283 to 284° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06545009B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-900f5f31b306459bbe341562963f140f |
| Source note | uspto-grants-2003_04 |