HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,5-Trimethoxybenzaldehyde → HCID 53767826, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,5-Trimethoxybenzaldehyde | HCID 20525 | — |
| Reactant | Benzeneacetonitrile, 4-bromo- | HCID 27914 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53767826 | HCID 53767826 | 95.7% |
Reaction Steps
A mixture of 1.96 g (10.0 mmol) of 2,4,5-trimethoxybenzaldehyde (purchased from Lancaster), and 1.96 g (10.0 mmol) of 4-bromophenylacetonitrile (purchased from Tokyo Kasei) in 5 ml of ethanol (purchased from Kokusan Kagaku) was heated to dissolve. Two drops of 20% aqueous sodium hydroxide solution was then added and the reaction mixture was stirred over night at ambient temperature. To the resultant reaction mass was added ethanol and crushed, and the precipitate was collected and washed with ethanol twice and with hexane twice, and dried to give 3.58 g (yield: 95.6%) of α-cyano-4-bromo-2',4',5'-trimethoxystilbene (as a yellow crystalline).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574062 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-f1b7f8e88ef34803a14f33835eca83dd |
| Source note | uspto-grants-1996_11 |