HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiocyanic Acid → 4,5-Diphenyl-2-oxazolyl mercaptoacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiocyanic Acid | HCID 781 | — |
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | Benzoin | HCID 8400 | — |
| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4,5-Diphenyl-4-oxazolin-2-one | HCID 151245 | — |
| Reactant | HCID 178527826 | HCID 178527826 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 4,5-Diphenyl-2-oxazolyl mercaptoacetic acid | HCID 21408360 | — |
Reaction Steps
12 g. of 2-mercapto-4,5-diphenyl-oxazole (m.p. 252°-254°, from methanol; obtainable from 4,5-diphenyl-2-oxazolone and phosphorus pentasulfide in boiling xylene, or by the reaction of benzoin with HSCN) is dissolved in 100 ml. of DMF, and 1.2 g. of NaH is added thereto. The reaction mixture is agitated for 1.5 hours at room temperature. Then, 5.6 ml. of the ethyl ester of bromoacetic acid in 20 ml. of DMF is added dropwise thereto, and the reaction mixture is stirred for 2 hours at 80°. The mixture is then mixed with water and worked up as usual, thus obtaining the ethyl ester of 4,5-diphenyl-2-oxazolyl-mercaptoacetic acid, b.p. 207°-210°/0.1 mm.; m.p. 54°-56° (hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03933840 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-48d6f71e58f743a39566282b6eeb664d |
| Source note | uspto-grants-1976_01 |