HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4779Erstellt: 23. Oktober 2026
Salicylamide → 2-[(1-Methyl-3-pyrrolidinyl)oxy]benzamide
https://huagongshe.com/de/reaction/4779
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Salicylamide | HCID 5147 | — |
| Edukt | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Edukt | Sodium amide | HCID 24533 | — |
| Edukt | 1-Methyl-3-pyrrolidinol | HCID 93074 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-[(1-Methyl-3-pyrrolidinyl)oxy]benzamide | HCID 13726283 | — |
Reaktionsschritte
To 85.6 g (2.2 moles) of sodium amide in 1.5 liter of dry toluene was added 202 g (2 moles) of 1-methyl-3-pyrrolidinol so as not to exceed a temperature of 50° C. The mixture was then heated to 70° C. for 4.5 hours. The mixture was cooled and 381 g (2 moles) of o-toluenesulfonylchloride was added at a rapid drop while maintaining a temperature of 20°-30° C. with an ice bath. The mixture was stirred at room temperature for 2.5 hours and washed with water. The toluene solution was dried with sodium sulfate and concentrated. The residue, dissolved in 500 ml of dimethylformamide, was added to a reaction mixture prepared by adding 119 g (2.2 moles) of sodium methoxide and 274 g (2.0 moles) of salicylamide to one liter of dimethylformamide and the mixture was worked up as in preparation 1. Yield of product was 170 g (38%), m.p. 116°-118° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04727152 |
|---|
| Quelldatensatz | uspto-grants-1988_02 |
|---|
| ORD ID | ord-b0c0fc9ef6e847a68cadcb68fa16fa36 |
|---|
| Quellennotiz | uspto-grants-1988_02 |
|---|