Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Chloroprene | HCID 31369 | — |
| Edukt | Chloromaleic anhydride | HCID 66772 | — |
| Edukt | Dichloromaleic anhydride | HCID 70728 | — |
| Katalysator | Phenothiazine | HCID 7108 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Chlorobenzene | HCID 7964 | — |
| Produkt | 4-Chloro-3,6-dihydrophthalic anhydride | HCID 10986977 | 498,4% |
Reaktionsschritte
A 3-necked 50 mL flask was equipped with a pressure equalizing additional funnel, a thermocouple well with a thermocouple, a water cooled condensor and a magnetic stir bar. The flask was charged with 6.62 g (0.05 mol) of monochloromaleic anhydride contaminated with approximately 0.005 mol of dichloromaleic anhydride, 6.1 g of monochlorobenzene and 100 mg of phenothiazine. The contents of the flask were heated to 92° C. and 4.42 g (0.05 mol) of chloroprene was added over 15 to 30 minutes. HCl gas was observed evolving from the reactor. After 16 hours at 92° C., the solvent was removed in-vacuo and triturated with 10 mL of diethyl ether to yield 4.6 g (50% of theoretical) of 4-chloro-3,6-dihydrophthalic anhydride. High resolution mass spectrometry (MS) of the solid resulted in the following analysis: Calculated mass=183.99271; observed mass=183.9924. 13C and 1H nuclear magnetic resonance (NMR) spectra were consistent with the assigned structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05322954 |
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| Quelldatensatz | uspto-grants-1994_06 |
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| ORD ID | ord-4a0b8bc91ed94c54b4a3af367b25209d |
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| Quellennotiz | uspto-grants-1994_06 |
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