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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719691Generated: October 25, 2026

2-Mercaptoethanol → 4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/719691

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4'-(bromomethyl)-[1,1'-biphenyl]-2-carboxylateHCID 46830451—
Reactant4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl esterHCID 58610579—
SolventDimethylformamideHCID 6228—
Product4'-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl esterHCID 5861059442%

Reaction Steps

4′-(2-Hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester was prepared as described for 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid ethyl ester. 4′-Bromomethyl-biphenyl-2-carboxylic acid ethyl ester (4.1 g, 12.84 mmol, 1 eq.) in anhydrous DMF was treated with 2-mercaptoethanol (1.2 g, 15.41 mmol, 1.2 eq.) and potassium carbonate (5.32 g, 38.52 mmol, 3 eq.). When complete, the reaction was worked up and purified as described for 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl4-carboxylic acid ethyl ester to leave 4′-(2-hydroxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester (3.05 g, 42% yield) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132456B2
Source datasetuspto-grants-2006_11
ORD IDord-2c769b8dbf7f4965b24ec406c6459a81
Source noteuspto-grants-2006_11