HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Cyclopentyl 4-methylbenzene-1-sulfonate | HCID 317685 | — |
| Edukt | methyl N-(2-fluoro-4-chloro-5-hydroxyphenyl)carbamate | HCID 19042327 | — |
| Katalysator | Potassium Iodide | HCID 4875 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate | HCID 15766845 | 93,1% |
Reaktionsschritte
Methyl N-(2-fluoro-4-chloro-5-hydroxyphenyl)carbamate (1.64 Kg, 7.47 mol), cyclopentyl-p-toluenesulfonate (1.80 Kg, 7.48 mol), potassium carbonate (1.03 Kg, 7.46 mol) and potassium iodide (12.3 g, 1.0 mol %) were placed in a 10L three-necked flask equipped with a stirrer and a Dimroth funnel, and, after adding acetone (7.5 liters) as a solvent thereto, the mixture was refluxed under heating for4 hours. After completion of the reaction, the reaction solution was taken out, and 0.5N hydrochloric acid (20 liters) was added thereto while vigorously stirring. The precipitated methyl N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)carbamate as a white solid (2.0 Kg, 6.95 mol, 93.1% yield) was isolated by filtration and thoroughly dired.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05554581 |
| Quelldatensatz | uspto-grants-1996_09 |
| ORD ID | ord-2a4e3ab8cf6c471282fa64238545f162 |
| Quellennotiz | uspto-grants-1996_09 |