HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → N-Benzylideneaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Aniline | HCID 6115 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-Benzylideneaniline | HCID 10858 | — |
Reaction Steps
Benzaldehyde (0.20 mole) was treated with aniline (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 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-benzylideneaniline. m.p. 50°-51.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04176198 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-6ad16f172d4d43a7aa3952a1e6effa4c |
| Source note | uspto-grants-1979_11 |