HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxyisophthalaldehyde → 4-[6-(Biphenyl-4-yl)hexyloxy]-1,3-benzenedicarboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxyisophthalaldehyde | HCID 165106 | — |
| Reactant | HCID 19930253 | HCID 19930253 | — |
| Product | 4-[6-(Biphenyl-4-yl)hexyloxy]-1,3-benzenedicarboxaldehyde | HCID 19930290 | — |
Reaction Steps
4-[6-(biphenyl-4-yl)hexyloxy]-1,3-benzenedicarboxaldehyde (MS: M+NH4+ =400) was prepared from 5-formyl salicylaldehyde and 6-(biphenyl-4-yl)hexyl tosylate at a temperature of 150° C. using the method in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428065 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-7c10f8c078874c038df927dfc39a7656 |
| Source note | uspto-grants-1995_06 |