HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276243Erstellt: 25. Oktober 2026
Thiophosgene → 2-Ethyl-4-cyanophenyl isothiocyanate
https://huagongshe.com/reaction/276243
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Thiophosgene | HCID 10040 | — |
| Edukt | 4-Amino-3-ethylbenzonitrile | HCID 2735330 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-Ethyl-4-cyanophenyl isothiocyanate | HCID 18316102 | — |
Reaktionsschritte
To a solution of 4-amino-3-ethylbenzonitrile, (75 g, 0.51 mol) in toluene (1 L) was added thiophosgene, (43 mL, 0.56 mol, 1.1 equiv.) slowly via syringe. Within 5 min. a viscous slurry formed. The reaction mixture was heated to the reflux temp. and the viscosity diminished. The reaction mixture was heated at the reflux temp. for 5 h then allowed to cool to room temp. The resulting mixture was concentrated under reduced pressure and the residue was treated with CH2Cl2 (600 mL) and concentrated under reduced pressure to give 4-cyano-2-ethylphenyl isothiocyanate as a light tan crystalline solid (98 g, 100%): 1H NMR (DMSO-d6) δ1.18 (t, J=7.4 Hz, 3H), 2.69 (q, J=7.4 Hz, 2H), 7.55 (d, J=7.0 Hz, 1H), 7.75 (d, J=7.0 Hz, 2H), 7.84 (s, 1H); MS (CI-MS) m/z 189 ((M+H)+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06353006B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-b3db55aa994a4f63ac19e73ea3b366b8 |
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| Quellennotiz | uspto-grants-2002_03 |
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