HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl chloroformate → Ethyl 1-naphthylsulfonylcarbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Naphthalenesulfonamide | HCID 163571 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Methyl Ethyl Ketone | HCID 6569 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Ethyl 1-naphthylsulfonylcarbamate | HCID 21983856 | 67% |
Reaktionsschritte
A mixture of 1-naphthalene sulfonamide (769 mg, 3.67 mmol) and potassium carbonate (563 mg, 4.07 mmol) in 2-butanone (9 ml) was heated under reflux for 30 min. Ethyl chloroformate (430 mg, 3.96 mmol) was added dropwise and the resulting solution was heated under reflux for 3 h. The mixture was cooled and diluted with H2O (30 ml) and AcOEt (10 ml). The aqueous layer was collected and adjusted to pH 2 by addition of 1N HCl (aq). Extraction with AcOEt (2×20 ml) and concentration of the dried organic extracts afforded ethyl 1-naphthylsulfonylcarbamate (674 mg, 67%) as a white solid. 1H NMR (DMSO-d6): δ 12.35 (bs, 1H), 8.57 (1H, d, J 8.6), 8.29 (2H, m), 8.11 (1H, d, J 7.7), 7.71 (3H, m), 3.90 (2H, q, J 7.1), 0.99 (3H, t, J 7.1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07091209B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-16b875041d6e42ef88af956f49470849 |
| Quellennotiz | uspto-grants-2006_08 |