HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495020Generated: October 25, 2026
Dimethyl Disulfide → 1-Bromo-4-chloro-3-methylthio-2-fluorobenzene
https://huagongshe.com/reaction/495020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | 1-Bromo-4-chloro-2-fluorobenzene | HCID 137275 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-4-chloro-3-methylthio-2-fluorobenzene | HCID 66954829 | 94% |
Reaction Steps
A solution of 1-bromo-4-chloro-2-fluorobenzene (20.4 g, 0.100 mol) in THF (50 mL) was slowly added to LDA (0.125 mol) in THF (600 mL) at −50° C. After addition, the solution was warmed to −20° C. and then cooled to −50° C. A solution of dimethyldisulfide (18.8 g, 0.20 mol) in THF (50 mL) was then slowly added and the mixture was warmed to ambient temperature. The reaction was quenched with water (200 mL), extracted with ethyl acetate (2×150 mL), and the combined organic phases dried and concentrated. The residual red oil was purified by chromatography (5% ethyl acetate in hexanes) to give 1-bromo-4-chloro-3-methylthio-2-fluorobenzene (23.9 g, 0.094 mol): 1H NMR (CDCl3): δ 7.40 (m, 1H), 7.15 (dd, 1H), 2.50 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538214B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-2f37ce768c56439b818cbd84a60a39f1 |
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| Source note | uspto-grants-2009_05 |
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