HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561797Erstellt: 25. Oktober 2026
Dimethylformamide → 5-bromo-2-chloro-N-cyclopropylbenzamide
https://huagongshe.com/reaction/561797
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 5-Bromo-2-chlorobenzoic acid | HCID 33127 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | Cyclopropylamine | HCID 69828 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 5-bromo-2-chloro-N-cyclopropylbenzamide | HCID 4806983 | — |
Reaktionsschritte
To a toluene solution (1 M) of 5-bromo-2-chlorobenzoic acid (1 eq.) and DMF (1.2 eq.) was added at 0° C. oxalyl chloride (1.2 eq.) dropwise over 1 h. The resulting solution was stirred at 0° C. for 2 h before the volatiles were removed in vacuo. The resulting residue was taken up in dichloromethane (1 M), cooled to 0° C. and added sequentially cyclopropylamine (1.5 eq.) and Hunig's base (2 eq.) dropwise over 1 h. The resulting suspension was stirred at RT for 18 h. The reaction was quenched with 1 N HCl and extracted with dichloromethane. The combined organic extracts were dried over MgSO4, filtered and the filtrate concentrated in vacuo to ˜⅓ in volume. The resulting white suspension was added an equivalent volume of hexanes and the title compound was isolated via vacuum filtration.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08063105B2 |
|---|
| Quelldatensatz | uspto-grants-2011_11 |
|---|
| ORD ID | ord-ec6452fdf13347f698dfb0fc19b47127 |
|---|
| Quellennotiz | uspto-grants-2011_11 |
|---|