HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 470908Erstellt: 26. Oktober 2026
1,2-Dichloroethane → 2,3-Dichloro-4-fluoro-2,3-dihydrobenzo[b]thiophene-7-carbonitrile
https://huagongshe.com/reaction/470908
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Sulfuryl chloride | HCID 24648 | — |
| Edukt | 4-Fluoro-1-benzothiophene-7-carbonitrile | HCID 67006238 | — |
| Produkt | 2,3-Dichloro-4-fluoro-2,3-dihydrobenzo[b]thiophene-7-carbonitrile | HCID 68546843 | — |
Reaktionsschritte
Sulfuryl chloride (3.0 mL, 37.0 mmol) was added to a solution of 4-fluorobenzo[b]thiophene-7-carbonitrile (1.05 g, 5.93 mmol) in 1,2-dichloroethane (30 mL) at room temperature. The mixture was heated at 60° C. for 24 h and then the solvent was removed and the residue mixed with saturated aq. NaHCO3 solution and extracted with 10% EtOAc in hexanes. These extracts were then washed with saturated aq. NaHCO3 solution, water, brine and dried over Na2SO4. Concentration gave the crude 2,3-dichloro-4-fluoro-2,3-dihydrobenzo[b]thiophene-7-carbonitrile as a brown solid (1.57 g). 1H NMR (400 MHz, CDCl3, δ in ppm) 7.68 (dd, J=4.7, 8.6 Hz, 1H), 7.03 (t, J=8.2 Hz, 1H), 5.82 (s, 1H), 5.74 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08629167B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-0825316ff768430ebfd8a2db7730b882 |
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| Quellennotiz | uspto-grants-2014_01 |
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