HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → p-Toluenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Calcium Sulfate | HCID 24497 | — |
| Reactant | 4-(4-Aminophenyl)butanoic acid | HCID 27049 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | — |
| Product | 4-(4-Aminophenyl)butyric acid benzyl ester | HCID 54272448 | — |
Reaction Steps
A mixture of 8.14 g (0.455 mol) of 4-(p-aminophenyl)butyric acid, 34.1 ml of benzyl alcohol and 8.65 g (0.455 mol) of p-toluene sulfonic acid hydrate in 115 ml of carbon tetrachloride is heated overnight at reflux with the solvent return through a tower of Drierite (ca. 30 ml of partially powdered indicating Drierite). The partially cooled mixture is diluted to 600 ml with ethyl ether to give a precipitate which is collected to give 4-(4-aminophenyl)butyric acid benzyl ester, p-toluenesulfonate; m.p. 114°-115° C. This is used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155268 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-e95fcabc17b447648e9214af064343fe |
| Source note | uspto-grants-1992_10 |