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) is treated with aniline (0.20 mole) with vigorous stirring in a 1 l. Erlenmeyer Flask. After 15 mins., 33 cc of 95% ethanol is added and the reaction mixture is stirred vigorously for an additional 5 minutes. The reaction mixture is left standing at room temperature for 10 min.; then it is placed in an ice-bath for 0.5 hrs. The crystals which form are collected, washed with 95% ethanol and air-dried. Recrystallization from 85% ethanol gives N-Benzylideneaniline. m.p. 50°-51.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04152452 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-db9ab2a341874f189e1b1ea98f9200ac |
| Source note | uspto-grants-1979_05 |