HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 614666Erstellt: 25. Oktober 2026
Methyl vinyl ketone → Diethyl (3-oxobutyl)phosphonate
https://huagongshe.com/reaction/614666
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl vinyl ketone | HCID 6570 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Diethylphosphite | HCID 3780918 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | Diethyl (3-oxobutyl)phosphonate | HCID 14033 | — |
Reaktionsschritte
To 243 grams (1.76 moles) of diethyl phosphite stirred under nitrogen and protected by a drying tube was added a solution of sodium ethoxide prepared from 5.07 grams (0.22 mole) of sodium in 100 ml of anhydrous ethanol. Methyl vinyl ketone, 112 grams (1.60 moles), was then added at such a rate as to keep the temperature at 35°-40° C. The addition required about one hour. The reaction mixture was stirred for one-half hour after the addition was completed and was stripped to dryness in vacuo at 60° C./16 mm. The residue was taken up in 600 ml of chloroform, and the solution cooled to 15° C. and washed successively with dilute acid, water and saturated sodium chloride solution. After drying, the chloroform solution was distilled to yield 112 grams of diethyl 3-oxobutylphosphonate as a colorless liquid, B.P. 106° C./0.05 mm, nD 25 1.4340. VPC indicated that the product was 90% pure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04145510 |
|---|
| Quelldatensatz | uspto-grants-1979_03 |
|---|
| ORD ID | ord-2235a397e2da43c799ab5315f944fab1 |
|---|
| Quellennotiz | uspto-grants-1979_03 |
|---|