HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Carbon Disulfide → 2-((Butylsulfanyl)carbonothioyl)sulfanyl)propanoic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | 1-Dodecanethiol | HCID 8195 | — |
| Edukt | 2-Bromopropionic acid | HCID 11729 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Katalysator | Tetrapropylammonium bromide | HCID 74745 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-((Butylsulfanyl)carbonothioyl)sulfanyl)propanoic acid | HCID 59347154 | 111,7% |
Reaktionsschritte
Dodecanethiol (2.50 g, 12.5 mmol), acetone (40 mL), and tetrapropylammonium bromide (0.27 g, 0.10 mmol) were added to a solution of sodium hydroxide (0.50 g, 12.5 mmol) in water (5 mL). The resulting solution was cooled in an ice bath and treated with carbon disulfide (0.75 mL, 0.95 g, 12.5 mmol). After 20 min, 2-bromopropanoic acid (1.91 g, 12.5 mmol) was added and the mixture was stirred at ambient temperature for 12 h. The solution was evaporated to ¼ volume and slowly acidified with 2 M hydrochloric acid (50 mL), then further diluted with water (150 mL). The resulting solid was collected and recrystallised from ether/light petroleum to give the title compound (15, R3=C12H25) as yellow crystals (3.33 g, 76%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07745553B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-cbdd9b4994364bda8b1573b9e3f599bd |
| Quellennotiz | uspto-grants-2010_06 |