Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013148Generated: October 31, 2026

Methyl iodide → 2-[(Methylsulfanyl)methyl]-1,1'-biphenyl

https://huagongshe.com/reaction/1013148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 21610890HCID 21610890—
SolventMethanolHCID 887—
SolventSodium MethoxideHCID 10942334—
Product2-[(Methylsulfanyl)methyl]-1,1'-biphenylHCID 2308912077%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of biphenyl-2-yl-methanethiol (4 g, 20 mmol) in methanol (27 mL) and sodium methoxide in methanol (0.5 M, 40 mL) was heated at 60° C. for 0.5 h, cooled, treated with methyl iodide (3.7 mL, 60 mmol) and re-heated at 60° C. for 0.5 h. After cooling to room temperature, the reaction mixture was quenched with ice-water, acidified (pH˜2) and extracted with ethyl acetate (3×50 mL). Combined organic layer was washed with water (1×50 mL) and brine (1×50 mL), dried (MgSO4), and concentrated to give a crude product that was passed through a bed of silica (solvent: ethyl acetate) to give 3.3 g of 2-methylsulfanylmethyl-biphenyl (yellow oil) that was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981907B2
Source datasetuspto-grants-2011_07
ORD IDord-e3aa70915ad8463ebf2b18ee2138c9e0
Source noteuspto-grants-2011_07