HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Buten-2-ol → HCID 22670696, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Buten-2-ol | HCID 11716 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 22670694 | HCID 22670694 | — |
| Product | HCID 22670696 | HCID 22670696 | 80.5% |
Reaction Steps
To a stirred solution of 2-(acetylthiomethyl)hexanal (32.6 g, 0.173 mole) in 325 ml of xylenes in a 500-mL RBF fitted with a Dean-Stark trap is added 2-hydroxy-3-butene (22.5 mL, 0.259 mole), followed by pyridinium p-toluenesulfonate (4.34 g, 0.017 mole) at room temperature under nitrogen. The mixture is heated to reflux overnight. After cooling to room temperature, the xylenes solution is washed with 300 mL of saturated NaHCO3 solution. The aqueous phase is extracted with 300 mL of ethyl acetate. The combined organic extract is washed with 200 mL of brine and 200 mL of water. After removing solvents, the product is obtained by vacuum distillation (157-160° C./1.5 mmHg) in 80.5% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794544B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-00bf24b172cd450d9e7268632c60a2ef |
| Source note | uspto-grants-2004_09 |