HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzylamine → (E)-2,4,6-Trimethoxystyryl 4-Methoxy-3-Nitrobenzyl sulfone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | 2,4,6-Trimethoxybenzaldehyde | HCID 70019 | — |
| Edukt | 2-((4-Methoxy-3-nitrobenzyl)sulfonyl)acetic acid | HCID 40427067 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | (E)-2,4,6-Trimethoxystyryl 4-Methoxy-3-Nitrobenzyl sulfone | HCID 11502726 | 28% |
Reaktionsschritte
To a solution of 4-methoxy-3-nitrobenzyl sulfonylacetic acid (4.5 g, 15.5 mmol) in 30 mL of glacial acetic acid was added 2,4,6-trimethoxybenzaldehyde (3.05 g, 15.5 mmol) and a catalytic amount of benzylamine (0.6 mL). The resulting mixture was heated at reflux temperature for 6 h. The reaction mixture was then concentrated under reduced pressure to yield a gummy material. The gum was triturated with 2-propanol to yield a solid product. The solid product was recrystallized from a mixture of acetic acid and 2-propanol to provide the 2-((E)-2-(4-methoxy-3-nitrobenzylsulfonyl)vinyl)-1,3,5-trimethoxybenzene product in 28% yield. m.p. 186-187° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08106033B2 |
| Quelldatensatz | uspto-grants-2012_01 |
| ORD ID | ord-e7f2ac0ae87647c08cf8e3d13cfce0df |
| Quellennotiz | uspto-grants-2012_01 |