HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54496Generated: October 25, 2026
Benzyl Alcohol → p-Toluenesulfonic acid
https://huagongshe.com/reaction/54496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Pipecolic acid, (-)- | HCID 439227 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2,3-Dihydroxybutanedioate | HCID 3806114 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | 185.5% |
Reaction Steps
To a slurry of 7.3 g (26.14 mmol) of the tartrate salt of (S)-pipecolic acid (Egbertson M. and S. J. Danishefsky, J. Org. Chem. 54:11 (1989) in 75 mL of dry benzene was added 13.5 mL (0.13 mol) of benzyl alcohol and 5.48 g (28.8 mmol) of p-toluenesulfonic acid monohydrate. The reaction mixture was heated at reflux under a Dean-Stark trap for 2 h and then cooled to room temperature. The solution was then diluted with 400 mL of ether and stirred overnight at 4° C. The resulting white solid was collected on a filter, washed with hexane and dried in vacuo to give 9.2 g (90%) of the p-toluenesulfonic acid salt of benzyl pipecolate (14). 1H NMR (300 MHz, D2O) δ 7.63 (d), 7.41 (s), 7.28 (d), 5.26 (ABq), 4.8 (s), 4.03 (dd), 3.92 (dd), 3.51-3.39 (m), 3.15-2.93 (s), 2.40 (s), 2.36-2.24 (m), 1.98-1.53 (m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05622970 |
|---|
| Source dataset | uspto-grants-1997_04 |
|---|
| ORD ID | ord-8b1914876ed14971ac26a0132645feb3 |
|---|
| Source note | uspto-grants-1997_04 |
|---|