HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52130Erstellt: 26. Oktober 2026
Triethylamine → N,N-diethyl-3-(N',N'-diethylthiocarbamoyloxy)picolinamide
https://huagongshe.com/reaction/52130
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Diethylthiocarbamoyl chloride | HCID 66607 | — |
| Edukt | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Edukt | N,N-diethyl-3-hydroxypyridine-2-carboxamide | HCID 3020810 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N,N-diethyl-3-(N',N'-diethylthiocarbamoyloxy)picolinamide | HCID 19963243 | 83% |
Reaktionsschritte
258.3 g (1.33 mol) of 3-hydroxy-N,N-diethylpicolinamide are introduced into 1 l of dimethylpropyleneurea and 213.2 ml (1.53 mol) of triethylamine at 0° C., and 222 g (1.464 mol) of diethylthiocarbamoyl chloride are introduced in the form of a solid. After the reaction mixture has been stirred for 2 hours at 0° C., it is poured into 2 l of water and extracted three times using ethyl acetate, the ethyl acetate phases are washed five times using 500 ml of water in each case, and the combined organic phases are dried over Na2SO4 and concentrated in vacuo at 60° C. Recrystallization from Et2O/hexane gives 341 g (83%) of brown crystals, m.p. 70°-72° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616590 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-7f4daed40d314eedb8125aa00e940a83 |
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| Quellennotiz | uspto-grants-1997_04 |
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