Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Thiophosgene | HCID 10040 | — |
| Edukt | Calcium Carbonate | HCID 10112 | — |
| Edukt | 6-Amino-2,4-dimethyl-3-pyridinecarbonitrile | HCID 3793299 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 6-Isothiocyanato-2,4-dimethylnicotinonitrile | HCID 18316201 | 93,3% |
Reaktionsschritte
A suspension of 6-amino-3-cyano-2,4-dimethylpyridine (0.1 g, 0.68 mmol) in CH2Cl2 (1 mL) was added to a vigorously stirred mixture of CaCO3 (0.41 g, 4.11 mmol) in a 1:2 water:CH2Cl2 mixture (9 mL total) at room temp. The reaction mixture was cooled to 0° C. and thiophosgene (0.09 g, 0.78 mmol) was added dropwise. The resulting mixture was allowed to warm to room temp and was stirred overnight. The resulting aqueous layer was back-extracted with CH2Cl2 (3×10 mL). The combined organic layers were washed with water (10 mL), dried (MgSO4) and concentrated under reduced pressure. The residue was purified by chromatography (SiO2, 10% EtOAc/hex) to give 2,4-dimethyl-3-cyano-6-pyridyl isothiocyanate (0.12 g, 91%): CI-MS m/z 190 ((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-2e90a8d951224d7f91b9854854bc5ed9 |
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| Quellennotiz | uspto-grants-2002_03 |
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