HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109822Generated: October 27, 2026
Hydrochloric Acid → 4-Chloro-3,6-dihydrophthalic anhydride
https://huagongshe.com/reaction/1109822
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-Chloro-3,6-dihydrophthalic anhydride | HCID 10986977 | — |
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 50 mg of phenothiazine. 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 multiple distilled into two fractions resulting in the isolation of 12.08 g of 4-chloro-3,6-dihydrophthalic anhydride which was identified by 13C 1H NMR and MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05322954 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-f5fff1231f7f429498d830b92d4add89 |
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| Source note | uspto-grants-1994_06 |
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