HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → Terephthaloyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Terephthalic Acid | HCID 7489 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Terephthaloyl chloride | HCID 7488 | — |
| Product | Dimethyl terephthalate | HCID 8441 | — |
Reaction Steps
Following the general procedure of Example 1 for the preparation of the diacid chloride, 10.31 parts of terephthalic acid were added to a mixture of 10.57 parts pyridine and 14.5 parts phosgene in 200 parts dry 1,2-dichloroethane at 25° to 30° C. The ratio of equivalents of pyridine base/COOH acid group was 1.08. After carrying out the reaction and esterifying the resulting diacid chloride by the procedure described in Example 1, a 95% yield of theory of dimethyl terephthalate was obtained corresponding to a 95% yield of theory of terephthaloyl chloride formed initially in the reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04129594 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-1802ca8856d748ad8fe7e7ccb16c48f6 |
| Source note | uspto-grants-1978_12 |