HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276213Generated: October 29, 2026
Sodium methanethiolate → 2-Chloro-4-iodobenzyl methyl sulfide
https://huagongshe.com/reaction/276213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 1-(Bromomethyl)-2-chloro-4-iodobenzene | HCID 22058683 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-4-iodobenzyl methyl sulfide | HCID 18316981 | 97.7% |
Reaction Steps
A solution of 2-chloro-4-iodobenzyl bromide (4.82 g, 14.54 mmol) in N,N-dimethylformamide (30 mL) was treated with sodium thiomethoxide (2.04 g, 29.08 mmol). After the addition, the solution became cloudy and turned to a yellow color. The resulting reaction mixture was stirred for 3 h at 25° C. The reaction mixture was then diluted with ethyl acetate (100 mL). The organic layer was washed successively with water (2×100 mL) and a saturated aqueous sodium chloride solution (1×100 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to afford 2-chloro-4-iodobenzyl methyl sulfide (4.24 g, 97%) as a colorless oil which was used without further purification: EI-HRMS m/e calcd for C8H8CIIS (M+) 297.9080, found 297.9078.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06353111B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-5536b223004b41d781ecb6ecdc56b4c2 |
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| Source note | uspto-grants-2002_03 |
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