HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13060845, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | Bromo(phenyl)acetic acid | HCID 97919 | — |
| Reactant | Ammonium dithiocarbamate | HCID 11083854 | — |
| Reactant | HCID 178527837 | HCID 178527837 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13060845 | HCID 13060845 | 58% |
Reaction Steps
A mixture of 10.0 g. (0.044 m.) 4-(4-chlorophenyl)-2-mercaptothiazole (prepared by the reaction of α-bromo-4-chloroacetophenone with ammonium dithiocarbamate) and 10.0 g. (0.04 m.) α-bromophenylacetic acid in 200 ml. of acetone and 40 ml. each of glacial acetic acid and acetic anhydride is heated for 2 hours. After the solvents are removed, the residual solid is triturated with acetone and the resulting solid collected. 10 g. (58% yield) of the title product is obtained, m.p. 160°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04327221 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-5875f1818272432c94a097031811a804 |
| Source note | uspto-grants-1982_04 |