HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2249365Erstellt: 26. Oktober 2026
Dimethyl Disulfide → 1-Bromo-4-chloro-3-methylthio-2-fluorobenzene
https://huagongshe.com/reaction/2249365
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Disulfide | HCID 12232 | — |
| Edukt | 1-Bromo-4-chloro-2-fluorobenzene | HCID 137275 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Bromo-4-chloro-3-methylthio-2-fluorobenzene | HCID 66954829 | 94% |
Reaktionsschritte
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. and a solution of dimethyldisulfide (18.8 g, 0.20 mol) in THF (50 mL) was slowly added and the mixture was warmed to ambient temperature. The reaction was quenched with water (200 mL) and extracted with ethyl acetate (2×150 mL) and the combined organic phases dried (sodium sulfate) and concentrated. The residual red oil was purified by chromatography (5% ethyl acetate in hexanes) to give 1-bromo-4-chloro-2-fluoro-3-(methylthio)benzene (23.9 g, 0.094 mol): 1H NMR (CDCl3): δ 7.40 (m, 1H), 7.15 (dd, 1H), 2.50 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07314849B2 |
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| Quelldatensatz | uspto-grants-2008_01 |
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| ORD ID | ord-297d85e8d8e74edb85e3e771370536d0 |
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| Quellennotiz | uspto-grants-2008_01 |
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