HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636029Generated: October 30, 2026
p-Toluenesulfonic acid → 2-(4-Methoxyphenyl)-4-(R)-undecyl-[1,3]dioxane
https://huagongshe.com/reaction/1636029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | p-(Dimethoxymethyl)anisole | HCID 75140 | — |
| Reactant | (R)-1,3-dihydroxytetradecane | HCID 11791041 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Methoxyphenyl)-4-(R)-undecyl-[1,3]dioxane | HCID 23556660 | 99.3% |
Reaction Steps
p-Toluenesulfonic acid (152 mg, 0.80 mmol) and 4-methoxybenzaldehyde dimethylacetal (2.9 g, 16.0 mmol) was added to a solution of (R)-1,3-dihydroxytetradecane (1.85 g, 8.0 mnuol) in dimethylformamide (20 ml) and the mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure. The residue was diluted with ethyl acetate. The ethyl acetate layer was successively washed with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution, dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using cyclohexane:ethyl acetate=9:1 as the eluant to give the desired product (2.78 g, yield 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06511965B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-77fec4c6531c459cb074f813e19b88a2 |
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| Source note | uspto-grants-2003_01 |
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