HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methyl-4-anisaldehyde → 1-Methoxy-2-methyl-4-[2-(4-nitrophenyl)ethenyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methyl-4-anisaldehyde | HCID 122936 | — |
| Reactant | Diethyl 4-nitrobenzylphosphonate | HCID 256065 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Methoxy-2-methyl-4-[2-(4-nitrophenyl)ethenyl]benzene | HCID 53960065 | 47.6% |
Reaction Steps
Sodium ethoxide (prepared from 0.70 g of Na and 30 mL of ethanol) was added to an ice-cold mixture of diethyl p-nitrobenzylphosphonate (9.09 g, 0.033 mole) and 3-methyl-p-anisaldehyde (5.0 g, 0.033 mole) in ethanol (about 100 mL). The resulting mixture was stirred overnight. The solid product was filtered, washed with ethanol and vacuum dried to give MMONS, 3-methyl-4-methoxy-4'-nitrostilbene (4.946 g, 0.0157 mole, 47.6% yield, m.p. 109°-111° C.). Recrystallization of MMONS from chloroform/ethanol gave crystals suitable for x-ray analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985178 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-a4a5c24b24814e31944ce154b7544aab |
| Source note | uspto-grants-1991_01 |