HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Malononitrile → HCID 178450345, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Malononitrile | HCID 8010 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Dibutyl squarate | HCID 65108 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | HCID 178450345 | HCID 178450345 | 56,4% |
Reaktionsschritte
2.16 ml (10 mmol) of 3,4-dibutoxy-3-cyclobutene-1,2-dione (2b) was dissolved in 20 ml of anhydrous benzene, and 660 mg (10 mmol) of malonodinitrile was added under stirring. Then, 1.65 ml (12 mmol) of triethylamine was added dropwise for 5 min followed by 10 ml of anhydrous benzene. The obtained emulsion is stirred for 30 min at room temperature. The solvent is removed using a rotary evaporator. The yellow oiled residue is treated three times with ether to give crude product 2d (1.8 g, 56%), 1H-NMR (DMSO-d6): δ 10.15–9.55 (1H, broad s, NH+), 4.59 (2H, t, 6.7 Hz, OCH2), 3.07 (6H, q 7.4, 14.5 Hz, N(CH2CH3)3), 1.77–1.58 (2H, m, CH2), 1.48–1.26 (2H, m, CH2), 1.18 (9H, t, 7.3 Hz, N(CH2CH3)3), 0.90 (3H, t, 7.4 Hz, CH3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07250517B2 |
| Quelldatensatz | uspto-grants-2007_07 |
| ORD ID | ord-e2e5d3fab79d4541a316c228b7dd659f |
| Quellennotiz | uspto-grants-2007_07 |