HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2296818Erstellt: 25. Oktober 2026
Trichloroacetonitrile → 2,4-Difluorobenzyl trichloroacetimidate
https://huagongshe.com/reaction/2296818
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trichloroacetonitrile | HCID 11011 | — |
| Edukt | 2,4-Difluorobenzyl alcohol | HCID 91867 | — |
| Katalysator | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Potassium Hydroxide | HCID 14797 | — |
| Produkt | 2,4-Difluorobenzyl trichloroacetimidate | HCID 11077074 | 92% |
Reaktionsschritte
Tetrabutyl ammonium hydrogen sulphate (15 mg) was added to 2,4-difluorobenzylalcohol (1.0 g, 6.94 mmol) in CH2Cl2 (10 ml) and KOH (50%, 10 ml). This mixture was cooled to −15° C. prior to the addition of trichloroacetonitrile (1.2 ml, 8.32 mmol). After 30 min at −15° C. and 3 h at ambient temperature the phases were separated. The aqueous phase was extracted twice with CH2Cl2. The combined organic phases were dried with MgSO4 and reduced to one third. The residue was filtered through celite and concentrated to give the crude 2,4-difluorobenzyl trichloroacetimidate (1.83 g, 92%) as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06489364B2 |
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| Quelldatensatz | uspto-grants-2002_12 |
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| ORD ID | ord-28cd121bda794ab8b9cb5eef5712f152 |
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| Quellennotiz | uspto-grants-2002_12 |
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