HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzaldehyde → HCID 15641097, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | 1,2,4-Butanetriol | HCID 18302 | — |
| Katalysator | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | HCID 15641097 | HCID 15641097 | 52,5% |
Reaktionsschritte
A mixture of 1,2,4-butanetriol (3.0 g, 28.3 mmol) and benzaldehyde (11.48 ml, 113 mmol) in dry toluene (50 mL) with p-toluenesulfonic acid monohydrate (0.269 g, 1.413 mmol) was heated under reflux in a Dean-Stark apparatus. After ˜1 h, the solution was washed with sat. aq NaHCO3, dried and concentrated under high vac to remove most of the benzaldehyde. Chromatography gave syrupy title compound (2.88 g, 14.83 mmol, 52.5% yield). The NMR's were the same as reported (Tetrahedron Asymm. 1996, 7, 3209-3246).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08853224B2 |
| Quelldatensatz | uspto-grants-2014_10 |
| ORD ID | ord-02b36c42d66346ff9c6707989ca20401 |
| Quellennotiz | uspto-grants-2014_10 |