HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Terephthaloyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| 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 9, but using more concentrated reaction media, a slurry of 8.22 parts terephthalic acid in 50 parts dry dichloromethane was added to a stirred mixture of 8.85 parts pyridine and 10.46 parts phosgene in 80 parts dry dichloromethane at 24° to 30° C. The ratio of equivalents of pyridine base/COOH acid group was 1.13. After carrying out the reaction and esterifying the resulting diacid chloride by the procedure as described in Example 1, a quantitative yield of dimethyl terephthalate was formed corresponding to a quantitative yield 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-b817d0b0a04245fc862259abd8f7a6b3 |
| Source note | uspto-grants-1978_12 |