HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591352Generated: October 31, 2026
Hydrogen Bromide → 4-Chlorophthalic anhydride
https://huagongshe.com/reaction/1591352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | HCID 54187688 | HCID 54187688 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 4-Chlorophthalic anhydride | HCID 67044 | 86% |
Reaction Steps
A mixture of 93 g (0.5 moles) of 4-chlorotetrahydrophthalic anhydride and 30 g of monochlorobenzene was heated and maintained at 105° C. TO 135° C. while 80 g (0.5 moles) of bromine was added over a three hour period. Simultaneously, chlorine gas (0.5 moles) was added to the vapor space above the organic liquid. As the HBr off-gas from the reaction of bromine with 4-chlorotetrahydrophthalic anhydride exited, it contacted the chlorine gas and the resultant bromine was condensed back into the organic liquid phase for reuse. A total of 36.45 g (0.5 moles) of chlorine were consumed during this time. The reaction mixture was finally heated to 165°-175° C. for an additional 5 hours. The crude reaction mixture was distilled resulting in isolation of 86% of 4-chlorophthalic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05206391 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-48602eeda35d4c2aad11f873f392888d |
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| Source note | uspto-grants-1993_04 |
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