HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Acetylbutyric acid → Pentafluorophenyl 5-oxohexanoate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Acetylbutyric acid | HCID 18407 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Pentafluorophenyl Trifluoroacetate | HCID 4327891 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Pentafluorophenyl 5-oxohexanoate | HCID 86609189 | 79,3% |
Reaktionsschritte
5-Oxohexanoic acid (2.6 g; 20 mmol) was dissolved in CH2Cl2 (50 mL). N,N-Diisopropylethylamine (10.4 mL, 60 mmol) was added followed by pentafluorophenyl trifluoroacetate (3.61 mL; 21 mmol). The reaction mixture was kept at room temperature for 1 hour and evaporated. The residue was resuspended in EtOAc:Hexanes (1:1) and loaded on a silica gel column (5×20 cm) equilibrated and developed with the same mixture. Fractions containing the product (14) (Rf˜0.7) were pooled and concentrated to give 4.7 g (79%) of yellowish oil after drying in vacuum. 1H NMR (CDCl3) δ 2.05 (m, 2H), 2.18 (s, 3H), 2.61 (t, 2H), 2.74 (t, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07476735B2 |
| Quelldatensatz | uspto-grants-2009_01 |
| ORD ID | ord-9c7fa08c558c4dcab32dedbbae5a14d7 |
| Quellennotiz | uspto-grants-2009_01 |