HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109823Generated: October 26, 2026
Hydrochloric Acid → 4-Chlorophthalic anhydride
https://huagongshe.com/reaction/1109823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Chloroprene | HCID 31369 | — |
| Reactant | Chloromaleic anhydride | HCID 66772 | — |
| Reactant | Dichloromaleic anhydride | HCID 70728 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chlorophthalic anhydride | HCID 67044 | 80% |
Reaction Steps
A 3-necked 50 mL flask was equipped with a pressure equalizing addition funnel, a thermocouple well with thermocouple, a water cooled condensor and a magnetic stir bar. The flask was charged with 13.2 g (0.10 mol) of a 90/10 GC area % mixture of monochloromaleic anhydride and dichloromaleic anhydride and 100 mg of phenothiazine and 0.5 g of activated carbon. The contents of the flask were heated to 80 to 130° C. and 8.8 g (0.1 mol) of chloroprene was added over 15 to 30 minutes. HCl gas was observed evolving from the reactor. After 6 hours at 130° C. the contents of the flask were sparged with oxygen for 2 hours between 130° and 150° C., filtered hot, and multiple distilled into two fractions resulting in the isolation of 13.2 g (80% of theoretical) of 4-chlorophthalic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05322954 |
|---|
| Source dataset | uspto-grants-1994_06 |
|---|
| ORD ID | ord-c5705182af3645479a36841d24a96591 |
|---|
| Source note | uspto-grants-1994_06 |
|---|