HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid | HCID 21899992 | — |
| Reactant | 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester | HCID 58610596 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid | HCID 21899991 | 98.2% |
Reaction Steps
3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid was synthesized as described for 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid. 3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester (0.80 g, 2.04 mmol, 1 eq.) in 30% aqueous THF was treated with lithium hydroxide (0.15 g, 6.12 mmol, 3 eq.). When complete, the reaction was worked up as described leaving 3′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid (0.73 g, 98% yield) as an orange oil that solidified on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132456B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-2d3e559e87084310ab36059feaffe221 |
| Source note | uspto-grants-2006_11 |