Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | O-Phenylenediamine | HCID 7243 | — |
| Edukt | 4-Cyanothiazole | HCID 15069 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Thiabendazole | HCID 5430 | 89,3% |
Reaktionsschritte
The product, thiabendazole, precipitated as it was formed in the reaction mixture. The reaction was monitored by gas chromatography and determined to be complete when the peaks corresponding to o-phenylenediamine and 4-cyanothiazole were negligible. The reaction mass was allowed to cool to 50° C. and 150 ml of 50° C. deionized water was added to thin the mixture before being vacuum filtered using a medium fritted glass filter. The solid product was washed four times with 300 ml portions of deionized water. The washed precipitate was dried overnight in a vacuum oven under 15-20" Hg and at a temperature of 80°-90° C. A total of 89.77 grams of thiabendazole were obtained which corresponds to an 89.3% yield. The color of dry thiabendazole was cream. High Performance Liquid Chromatography (HPLC) using a Hewlett-Packard Model 1090M showed that the purity was 98.77% (based on % area).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05310924 |
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| Quelldatensatz | uspto-grants-1994_05 |
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| ORD ID | ord-1942a8dab9ce4763b2b90060eddba93b |
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| Quellennotiz | uspto-grants-1994_05 |
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