HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-2-methylaniline → N-(o-Chlorobenzylidene)-2-methyl-3-chloroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-2-methylaniline | HCID 6894 | — |
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(o-Chlorobenzylidene)-2-methyl-3-chloroaniline | HCID 13017551 | — |
Reaction Steps
o-Chlorobenzaldehyde (0.20 mole) was treated with 3-chloro-2-methylaniline (0.20 mole) 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 mins. The reaction mixture was left standing at room temperature for 10 mins., then it was placed in an ice-bath for 0.5 hr. The crystals which formed were collected, washed with 95% ethanol and air dried. Recrystallization from 85% ethanol gave N-(o-chlorobenzylidene)-3-chloro-2-methylaniline. m.p. 83°-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04176198 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-8697aaa5d6ba4de79d18df518c4263a8 |
| Source note | uspto-grants-1979_11 |