Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (R)-Solketal | HCID 736056 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21310391 | HCID 21310391 | 113.1% |
Reaction Steps
In a 6 liter reactor equipped with a condenser, a temperature probe and a dropping funnel are introduced 420 ml of demineralized water and 420 g (10.5 mol) of sodium hydroxide in pellets. To the solution, stirred at 20° C., are added 2.3 1 of dichloromethane, 396 g (3.00 mol) of (R)-2,2-dimethyl-1,3-dioxolane-4-methanol ([α]D20 =-11° ; c=4; methanol) and 20.5 g (0.090 mol) of benzyltriethylammonium chloride. 567 g (4.50 mol) of dimethyl sulfate are then added in 50 min, while keeping the temperature below 30° C. The mixture is stirred for 18 hours and then 1 liter of water is added. The organic phase is separated and washed with 0.5 1 of water. The aqueous phases are re-extracted with 3 1 of dichloromethane and the organic phases are then combined, filtered and concentrated by distillation under reduced pressure. 496 g of product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06143772 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-207333c9e94f4107aeaf8221658d692e |
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| Source note | uspto-grants-2000_11 |
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