HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Benzylideneaniline → 6-Methoxy-2-[4-(2-phenylethenyl)phenyl]-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Benzylideneaniline | HCID 10858 | — |
| Reactant | 6-Methoxy-2-(4-methylphenyl)-1-benzofuran | HCID 18925544 | — |
| Product | 6-Methoxy-2-[4-(2-phenylethenyl)phenyl]-1-benzofuran | HCID 53746788 | — |
Reaction Steps
Following the procedure given in Example 1b 2-(p-tolyl)-6-methoxybenzofuran was interacted with an equimolar quantity or benzalaniline to produce 2-(4-stilbenyl)-6-methoxybenzofuran, which, when recrystallized from toluene, melted at 223.5°-225.5° C. The wavelength of maximum excitation of this compound was 371 nm., and the wavelength of maximum emission was 446 nm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03993645 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-0a1bbb0cf2b84648b1461b52e15fd399 |
| Source note | uspto-grants-1976_11 |