HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Mercaptoethanol → 3'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester | HCID 58610579 | — |
| Reactant | 3'-Bromomethyl-biphenyl-4-carboxylic acid ethyl ester | HCID 58610587 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester | HCID 58610598 | — |
Reaction Steps
3′-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester was synthesized as described for 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester. 3′-Bromomethyl-biphenyl-4-carboxylic acid ethyl ester (4.98 g, 15.6 mmol, 1 eq) in anhydrous DMF was treated with 2-mercaptoethanol (2.44 g, 31.20 mmol, 2 eq.) and potassium carbonate (6.47 g, 46.80 mmol, 3 eq.). When complete, the reaction was worked up as described leaving a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132456B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-f3ea096d400641448c348262cbcd3c2a |
| Source note | uspto-grants-2006_11 |