HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Pyridine → N-[3-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | 3-Aminobenzyl alcohol | HCID 80293 | — |
| Edukt | Benzoyl chloride, 4-(tetradecyloxy)- | HCID 9998158 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-[3-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamide | HCID 10003333 | 82,1% |
Reaktionsschritte
To a solution of 8.17 g of m-aminobenzyl alcohol and 16.14 g of pyridine in 200 ml of methylene chloride is added at 0° C. over 30 minutes a solution of 18 g of p-tetradecyloxybenzoyl chloride in 200 ml of methylene chloride. Stirring is continued for another 6 hours. An additional 400 ml of chloroform and water is added followed by warming to dissolve all the solids. The warm organic layer is separated and washed with dilute hydrochloric acid and saturated sodium bicarbonate. The warm organic layer is dried and filtered. The filtrate is diluted with an equal volume of hexane and cooled in a refrigerator overnight. The resulting solid is collected and air dried to give 18.4 g of the desired product as a white solid, m.p. 112°-115° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05231182 |
| Quelldatensatz | uspto-grants-1993_07 |
| ORD ID | ord-1d0883649c7d424994873662eac1dba4 |
| Quellennotiz | uspto-grants-1993_07 |