HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927813Generated: November 4, 2026
p-Toluenesulfonic acid → Methyl 2-(2-methoxyethyl)-5-methyl-1,3-dioxane-5-carboxylate
https://huagongshe.com/reaction/1927813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,1,3-Trimethoxypropane | HCID 84348 | — |
| Reactant | Propanoic acid, 3-hydroxy-2-(hydroxymethyl)-2-methyl-, methyl ester | HCID 87346 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 2-(2-methoxyethyl)-5-methyl-1,3-dioxane-5-carboxylate | HCID 68510063 | — |
Reaction Steps
51 mg of 4-toluenesulphonic acid are added to a solution of 400 mg of methyl 3-hydroxyl-2-(hydroxymethyl)-2-methylpropanoate and 362 mg of 1,1,3-trimethoxypropane in toluene, and the mixture is stirred at 80° C. for 4 hours. After addition of saturated sodium bicarbonate solution, the organic phase is separated off and dried over sodium sulphate, and the solvent is removed under reduced pressure. The residue is filtered through silica gel (mobile phase cyclohexane/ethyl acetate 4:1). This gives 478 mg of methyl 2-(2-methoxyethyl)-5-methyl-1,3-dioxane-5-carboxylate as a mixture of two isomeric forms in a purity of about 38% (LCMS).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183351B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-2d7f54ad89634a66a3c1b19286077fbd |
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| Source note | uspto-grants-2012_05 |
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