HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(2',3'-Dichlorophenyl)-2-nitroethylene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 2,3-Dichlorobenzaldehyde | HCID 35745 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(2',3'-Dichlorophenyl)-2-nitroethylene | HCID 3503654 | — |
Reaction Steps
28.0 g of 2,3-dichlorobenzaldehyde, 13.9 g of ammonium acetate, 13.9 ml of nitromethane and 120 ml of glacial acetic acid are refluxed for 2 hours. After cooling, the reaction mixture is poured onto ice and stirred for 30 minutes. The formed precipitate is then filtered off, washed with water and dried in vacuo to thus obtain the product in the form of slightly yellowish crystals, m.p. 89°-91° C. IR (CHCl3) in cm-1 : 1650 (C=C); 1530 and 1350 (NO2). NMR (CDCl3) in ppm: 7.2-7.7 (m, 4H); 8.50 (d,J=15 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04778901 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-dd5e63f6fc8b4053b59bc1acc0f5aa75 |
| Source note | uspto-grants-1988_10 |