HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561784Generated: October 26, 2026
Dimethyl Sulfone → 2-(3-Iodophenyl)ethyl methyl sulfone
https://huagongshe.com/reaction/561784
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfone | HCID 6213 | — |
| Reactant | 3-Iodobenzyl bromide | HCID 2759361 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Iodophenyl)ethyl methyl sulfone | HCID 57956087 | — |
Reaction Steps
To a solution of dimethyl sulfone (1 eq.) in 60 mL of anhydrous THF (0.2 M) was added, at −78° C., n-butyl lithium (1.6 M hexane solution, 1.2 eq.) over a period of 10 min. The resulting mixture was stirred at −78° C. for 1 h. To the now yellow solution was added, at −78° C., 3-iodobenzyl bromide (I eq.). The reaction mixture was then slowly warmed to RT over 16 h. The reaction was carefully quenched with 10% aq. HCl and extracted with ether. The combined organic extracts were washed with brine, dried over MgSO4 and filtered. Concentration of the filtrate in vacuo afforded a viscous oil. Purification of the crude product thus obtained by way of flash chromatography (SiO2, Hex→1:1 (v/v) Hex:EtOAc) followed by trituration with hexanes afforded the title compound as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063105B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-2919ee22e19842ef9a5b17369d850419 |
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| Source note | uspto-grants-2011_11 |
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