HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dichloroaniline → HCID 23333926, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dichloroaniline | HCID 12281 | — |
| Reactant | Methyl 4-Formylbenzoate | HCID 15294 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23333926 | HCID 23333926 | — |
Reaction Steps
p-Carbomethoxybenzaldehyde (0.20 moles) was treated with 3,5-dichloroaniline (0.20 moles) with vigorous stirring in a 1 liter Erlenmeyer Flask. After 15 mins., 33 cc. of 95% ethanol was added and the reaction mixture was stirred vigorously for an additional 5 minutes. The reaction mixture was left standing at room temperature for 10 min.; then it was placed in an ice bath for 0.5 hours. The crystals which formed were collected, washed with 95% ethanol, and air-dried. Recrystallization from 85% ethanol gave N-(p-carbomethoxybenzylidene)-3,5-dichloroaniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04200648 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-110f18219009481a92af082b00b32451 |
| Source note | uspto-grants-1980_04 |