HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Mercaptoethanol → 3'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-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-2-carboxylic acid ethyl ester | HCID 58610601 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester | HCID 58610591 | — |
Reaction Steps
3′-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester was prepared as described for 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester. 3′-Bromomethyl-biphenyl-2-carboxylic acid ethyl ester (5.4 g, 16.92 mmol, 1 eq.). in anhydrous DMF was treated with 2-mercaptoethanol (1.59 g, 20.30 mmol, 1.2 eq.) and potassium carbonate (7.02 g, 50.76 mmol, 3 eq.). When complete, the reaction was worked up as described leaving a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132456B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-9e037fe542164ff49d1650815e1a41c1 |
| Source note | uspto-grants-2006_11 |