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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 21610890 | HCID 21610890 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Methoxide | HCID 10942334 | — |
| Product | 2-[(Methylsulfanyl)methyl]-1,1'-biphenyl | HCID 23089120 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981907B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-e3aa70915ad8463ebf2b18ee2138c9e0 |
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| Source note | uspto-grants-2011_07 |
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