HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid | HCID 21899992 | — |
| Reactant | 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester | HCID 58610578 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid | HCID 21899977 | 65.5% |
Reaction Steps
4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid was prepared as described for 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid. 4′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester (3.75 g, 9.55 mmol, 1 eq.) in 30% aqueous THF was reacted with lithium hydroxide (0.69 g, 28.65 mmol, 3 eq.). When complete, the reaction was worked up as described leaving a light yellow solid which was recrystallized from acetone/diethyl ether to afford 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid (2.28 g, 65% yield) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132456B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-820298e8cce1427ba64559bdd5e6eece |
| Source note | uspto-grants-2006_11 |