HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 22670697, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Buten-2-ol | HCID 11716 | — |
| Reactant | HCID 14640309 | HCID 14640309 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22670697 | HCID 22670697 | — |
Reaction Steps
To a stirred solution of 2-(((4-methylphenyl)-sulfonyl)methyl)hexanal (5.63 g, 21 mmol) in 35 ml of toluene in a RBF fitted with a Dean-Stark trap is added 2-hydroxy-3-butene (10 mL, 115 mmol), followed by p-toluenesulfonic acid (0.13 g) at room temperature under nitrogen. The mixture is heated to reflux overnight. After cooling to room temperature, the toluene solution is washed with saturated NaHCO3 solution (2×10 mL), water (2×20 mL), brine (1×20 mL), and dried with MgSO4. After removing solvents, the product is obtained as a brownish oil in quantitative yield with a GC purity of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794544B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-5798f62f46be4fdc9a93f4c577f44f29 |
| Source note | uspto-grants-2004_09 |