HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Mercaptoethanol → 3'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Mercaptoethanol | HCID 1567 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester | HCID 58610579 | — |
| Edukt | Ethyl 3'-(bromomethyl)biphenyl-3-carboxylate | HCID 58610582 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester | HCID 58610580 | — |
Reaktionsschritte
3′-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester was synthesized as described for 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester. 3′-Bromomethyl-biphenyl-3-carboxylic acid ethyl ester (3.4 g, 10.65 mmol, 1 eq.) in anhydrous DMF was treated with 2-mercaptoethanol (1.0g, 12.78 mmol, 1.2 eq.) and potassium carbonate (4.42 g, 31.95 mmol, 3 eq.). When complete, the reaction was worked up as described leaving a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07132456B2 |
| Quelldatensatz | uspto-grants-2006_11 |
| ORD ID | ord-ee7beca2e30e4fa7adf83c8cbe4b7b1e |
| Quellennotiz | uspto-grants-2006_11 |