Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | Propanoic acid, 2,2,3,3,3-pentafluoro-, ethyl ester | HCID 67928 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Edukt | HCID 178472209 | HCID 178472209 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | HCID 178469142 | HCID 178469142 | 30,7% |
Reaktionsschritte
To a -78° C. solution of LDA (0.10 mol), prepared from 0.10 mol of n-BuLi and 14 ml (0.10 mol) of diisopropylamine in 70 ml ether was added a solution of 10.0 g (0.042 mol) of product of Example 34 in 20 ml of ether slowly to maintain a temperature below -60° C. After stirring for 30 minutes, the reaction mixture was treated with 21 ml (0.042 mol) of ethyl pentafluoropropionate. After stirring at -78° C. for 15 minutes, the reaction mixture was warmed to 10° C. in 0.5 hour and poured into 100 ml of water, and extracted with ether. The ether extract was extracted with 10% K2CO3. The combined aqueous layer and K2CO3 extract was acidified with concentrated HCl to give 4.73 g (29.5%) of beige solid; mp 115°-117° C. (dec). A 2.73 g (0.00709 mol) of the solid was heated in a kugelrohr pot at 130° C. for 0.5 hour. The distillate and residue were combined and dissolved in ether. The ether solution was dried (CaSO4) and concentrated to give 2.0 g (76.9%) of product as a solid; mp 36°-38° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04655816 |
|---|
| Quelldatensatz | uspto-grants-1987_04 |
|---|
| ORD ID | ord-b132052dda1a42b084f6d6e2749934bd |
|---|
| Quellennotiz | uspto-grants-1987_04 |
|---|