Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Phenothiazine | HCID 7108 | — |
| Edukt | Chloroprene | HCID 31369 | — |
| Edukt | Chloromaleic anhydride | HCID 66772 | — |
| Edukt | Dichloromaleic anhydride | HCID 70728 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-Chloro-3,6-dihydrophthalic anhydride | HCID 10986977 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05322954 |
|---|
| Quelldatensatz | uspto-grants-1994_06 |
|---|
| ORD ID | ord-f5fff1231f7f429498d830b92d4add89 |
|---|
| Quellennotiz | uspto-grants-1994_06 |
|---|