HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → HCID 20225450, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Allyloxybutyl-p-toluene sulfonate | HCID 86740343 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20225450 | HCID 20225450 | — |
Reaction Steps
4-allyloxybutyl-p-toluene sulfonate is reacted with p-hydroxybenzaldehyde in the presence of KOH and C2H5OH to form 4-(4-allyloxybutoxy)benzaldehyde which is reacted with malonic acid in the presence of pyridine to form p-(4-allyloxybutoxy)cinnamic acid. The acid is esterified with CH3OH and sulfuric acid to yield the methyl ester, namely methyl p-(4-allyloxybutoxy)cinnamic carboxylate. This methyl ester is then reacted with TosMIC in Et2O/DMSO in the presence of sodium hydride or other strong base to form the substituted pyrrole, represented as follows: ##STR7##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04543402 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-07c0314329e54620a1e7a11e2a346b8b |
| Source note | uspto-grants-1985_09 |