HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 178427655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 178511262 | HCID 178511262 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178427655 | HCID 178427655 | 92% |
Reaction Steps
A mixture of 10.0 g (63.6 mmol) of trans4-aminomethylcyclohexane-1-carboxylic acid, 25.1 g (132 mmol) of 4-toluenesulfonic acid, 50 mL (482 mmol) of benzyl alcohol, and 75 mL of toluene was heated to reflux under a N2 atmosphere using a Dean-Stark trap to collect water formed during the reaction. During reflux, all solids dissolved to leave a colorless solution. After 3 hours at reflux, the solution began to turn yellow. Heat was removed, and the flask allowed to cool to room temperature. The solids which separated out were collected and washed with diethyl ether. There was obtained 24.5 g (58.4 mmol, 92% yield) of product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046169 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-5b3914e476904243b05d04a8ebdff1bf |
| Source note | uspto-grants-2000_04 |