HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Z,E-1,4-Bis-(4-carboxy-styryl)-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Z,E-1,4-Bis-(4-carbo-tert.-butoxy-styryl)benzene | HCID 67828321 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Z,E-1,4-Bis-(4-carboxy-styryl)-benzene | HCID 67828586 | — |
Reaction Steps
131 g of Z,E-1,4-Bis-(4-carbo-tert.-butoxy-styryl)benzene are boiled under reflux with 6.5 g of p-toluenesulphonic acid in 1 l of toluene for 3 hours. The reaction product is evaporated to dryness and heated for a further 4 hours with 30 g of NaOH in 300 ml of water and 600 ml of ethanol. The ethanol is distilled off and the residue is acidified (conc. HCl) after dilution with water. The product is suction filtered and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05068300 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-599b23970bfd45388bcf042611b86e8e |
| Source note | uspto-grants-1991_11 |