HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 5-Hydroxy-4,6,7-trifluoro-3-(pentafluorobenzylidene)phthalide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Tetrafluorophthalic anhydride | HCID 69545 | — |
| Edukt | (Pentafluorophenyl)acetic acid | HCID 69553 | — |
| Edukt | 3,4,6-Trifluoro-5-hydroxyphthalic acid | HCID 10198587 | — |
| Lösungsmittel | Acetic anhydride triethylamine | HCID 21881581 | — |
| Produkt | 5-Hydroxy-4,6,7-trifluoro-3-(pentafluorobenzylidene)phthalide | HCID 73675640 | — |
Reaktionsschritte
A process for preparing 3,5,6-trifluoro-4-hydroxyphthalic acid used here as the starting material is described in Osadchii, S. A., Bakahash, V. A.; Zh. Org. Khim., Vol. 6 (8), p. 1636 (1970) (Chemical Abstract, 73, 109544p). According to this litrature, when tetrafluorophthalic anhydride and pentafluorophenylacetic acid are reacted in triethylamine-acetic anhydride, a triethylamine salt of 5-hydroxy-4,6,7-trifluoro-3-(pentafluorobenzylidene)phthalide is obtained. And, by treatment of the by-products of this reaction, 3,5,6-trifluoro-4-hydroxyphthalic acid is obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04831190 |
| Quelldatensatz | uspto-grants-1989_05 |
| ORD ID | ord-ed6bc3cba3af4f3bb2061a3dcb78b3a3 |
| Quellennotiz | uspto-grants-1989_05 |