HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2068548Erstellt: 26. Oktober 2026
Triethylamine → Ethyl 1-(4-cyclopropoxybenzamido)cyclopropanecarboxylate
https://huagongshe.com/reaction/2068548
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | Ethyl 1-aminocyclopropane-1-carboxylate hydrochloride | HCID 386203 | — |
| Edukt | 4-Cyclopropoxybenzoic acid | HCID 21452864 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Ethyl 1-(4-cyclopropoxybenzamido)cyclopropanecarboxylate | HCID 67234427 | 85% |
Reaktionsschritte
To a 0° C. suspension of 4-cyclopropoxybenzoic acid (24.5 g, 137.3 mmol) in dichloromethane (350 mL) containing 2 drops of DMF, slowly add oxalyl chloride (23.8 mL, 274.7 mmol). After addition, remove the cooling bath and stir for 2 hours. Concentrate the material to dryness under reduced pressure. Dissolve the residue in dichloromethane (500 mL), and then add ethyl 1-aminocyclopropanecarboxylate hydrochloride (Indofine #04-265, 24.9 g, 150.5 mmol) and triethylamine (57.2 mL, 410.4 mmol). Stir the mixture at ambient temperature for approximately 16 hours. Wash the mixture once with 10% NaHSO4 (250 mL). Separate the organic portion and extract the aqueous portion 2× with dichloromethane (200 mL). Combine the organic, dry over sodium sulfate, filter, and concentrate under reduced pressure. Purify the crude mixture by flash chromatography (0% to 45% EtOAc/Hex) to give the title compound (33.7 g, 85%): MS (m/z): 290 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08299061B2 |
|---|
| Quelldatensatz | uspto-grants-2012_10 |
|---|
| ORD ID | ord-66cf8552de9a4129b5ce6d2444e291c0 |
|---|
| Quellennotiz | uspto-grants-2012_10 |
|---|