HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663581Generated: October 30, 2026
Methanol → 2,2-Dimethyl-4-((phenylmethoxy)methyl)-1,3-dioxolane
https://huagongshe.com/reaction/1663581
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Solketal | HCID 7528 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,2-Dimethyl-4-((phenylmethoxy)methyl)-1,3-dioxolane | HCID 85795 | — |
Reaction Steps
To a 1000 ml round-bottom flask fitted with a thermometer, a nitrogen-introducing tube, and a stirrer were added 132.2 g (1.0 mol) of 2,2-dimethyl-1,3-dioxolane-4-methanol, 202.5 g (1.05 mol) of a 28% methanol solution of sodium methoxide, and 500 ml of toluene. With introduction of nitrogen thereinto, toluene was refluxed under reduced pressure for 1 hour to remove the methanol by evaporation. With maintaining the solution at 80° C., 126.6 g (1.0 mol) of benzyl chloride was added dropwise over a period of 2 hours using a dropping funnel, followed by another 2 hours of reaction. After completion of the reaction, the temperature was lowered to 60° C. and 10 g of KYOWAAD 600 was added, followed by 1 hour of stirring. After filtration of the reaction liquid, the solvent was removed and the residue was purified by distillation (b.p. 93-95° C./266 Pa) to obtain 4-(benzyloxymethyl)-2,2-dimethyl-1,3-dioxolane
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034981B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-5a3488a3e2e644f18b6aeec3c64332cc |
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| Source note | uspto-grants-2011_10 |
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