Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-(Dimethylamino)-2-propenal | HCID 79125 | — |
| Edukt | trans-4-(Dimethylamino)-3-buten-2-one | HCID 5369152 | — |
| Edukt | Borate(1-), tetrafluoro-, hydrogen, compd. with pyridine (1:1:1) | HCID 11019233 | — |
| Lösungsmittel | AcOH AcOAc | HCID 21895370 | — |
| Produkt | HCID 178467801 | HCID 178467801 | 96% |
Reaktionsschritte
Pyridinium tetrafluoroborate (2.21 g, 13.3 mmol) was added to a solution of (3E)-4-(dimethylamino)-3-buten-2-one (1.54 ml, 13.3 mmol) in 13.5 ml acetic anhydride/acetic acid (2:1). The resulting suspension was cooled to 0° C. and 3-dimethylaminoacroleine (1.33 ml, 13.3 mmol) was added over a period of 1 h under vigorous stirring and cooling with an ice bath receiving a red-brown precipitate. The cool reaction mixture was filtered and the remaining solid was washed with diethylether several times and dried under reduced pressure. The pentamethinium salt was obtained as orange crude product (2.69 g, 96%) and was used without any further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754111B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-cd552ca6e27549e988c610e8cce96ebb |
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| Quellennotiz | uspto-grants-2014_06 |
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