Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57184026 | HCID 57184026 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70292549 | HCID 70292549 | — |
Reaction Steps
0.8 g (5.2 mmol) of (1S)-3,4,5,5-tetramethyl-3-cyclohexen-1-ol was dissolved under N2 in 5 ml of absolute methylene chloride, the solution was cooled to 0° C. and 260 mg (1.04 mmol) of pyridinium p-toluenesulfonate, and then 0.45 mg (6.2 mmol) of ethyl vinyl ether were added. The mixture was subsequently stirred at 0° C. for 1 h and then poured into a saturated aqueous NaHCO3 solution, the mixture was extracted with methylene chloride, and the extract was dried over MgSO4 and concentrated. The residue was purified by distillation to yield 1.1 g (corresponding to 97% of theory) of the abovementioned product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06111125 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-2541252c4d1d4fe9824903e7aa414ffd |
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| Source note | uspto-grants-2000_08 |
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