HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → p-Toluenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | 1,4-Benzenediethanol | HCID 5013205 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | 43% |
Reaction Steps
To a stirred solution of the intermediate from Step A in THF (50 mL) was added DABCO (1.51 g, 13.5 mmol) and then p-toluenesulfonyl chloride (50 mL). The resulting mixture was stirred overnight at room temperature and then filtered to remove precipitated hydrochloride salts. The filtrate was concentrated under reduced pressure and DCM (50 mL) was added to the residue. The organic layer was then washed with water (1×100 mL), saturated NaCl (1×100 mL), dried over magnesium sulfate, filtered and the solvent removed under reduced pressure. The resulting material was purified by silica gel chromatography (70% EtOAc/hexane) to afford 1.25 g of the title intermediate (43% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250414B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-cba5fd562609417f808e72c6cc7c5bfb |
| Source note | uspto-grants-2007_07 |