HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetate → 1-(2,3,4-TRIMETHOXYPHENYL)-2-NITROPROPENE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetate | HCID 175 | — |
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | 2,3,4-Trimethoxybenzaldehyde | HCID 75006 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2,3,4-TRIMETHOXYPHENYL)-2-NITROPROPENE | HCID 620072 | 85.4% |
Reaction Steps
A mixture of 3.9 g of 2,3,4-trimethoxybenzaldehyde, 3.7 g of nitroethane, 2.5 g of Amberlite IR-45 acetate and 200 ml of toluene is refluxed for 20 hours while removing the resultant water. After the reaction is completed, the reaction mixture is filtered, and the filtrate is evaporated to remove solvent. The residue thus obtained is recrystallized from a mixture of isopropyl ether and hexane. 4.3 g of 1-(2,3,4-trimethoxyphenyl)-2-nitropropene are thereby obtained as yellow cubes. M.p. 57°-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04490392 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-875f3b0722264028a5c1a7c1dd44c11e |
| Source note | uspto-grants-1984_12 |