Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Diethylamine | HCID 8021 | — |
| Edukt | Methyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylate | HCID 12271748 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N,N-Diethylacrylamide | HCID 17583 | — |
Reaktionsschritte
7.2 parts 30% methanolic Na-methylate solution are added to 36.5 parts diethylamine. 77 parts 2-carbomethoxy-7-oxabicyclo(2,2,1)hept-5-ene are added drop-wise at 40° C. The reaction medium is then stirred for 15 hours at this temperature and neutralised with 4 parts concentrated hydrochloric acid. 100 parts methylene chloride and 50 parts water are added, the organic phase separated off, and the aqueous phase extracted 3 times with 25 parts methylene chloride in each instance. The combined organic phases are reduced in a rotary evaporator at a bath temperature of 90° C. and under a vacuum of 20 Torr. The residue is heated under a vacuum of 20 Torr to 110° to 120° C. (bath temperature 140° C.). On conclusion of the furane separation, the sedimentation temperature increases and the product distills over at the now lowered pressure. 21 parts N,N-diethylacrylamide with a boiling point of 55° C. at 1 Torr are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04605740 |
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| Quelldatensatz | uspto-grants-1986_08 |
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| ORD ID | ord-26fbb501dc83464bbb6d1b5292d80de1 |
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| Quellennotiz | uspto-grants-1986_08 |
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