HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250522Generated: October 26, 2026
Ethylene Glycol → 2-Methyl-2-(4-methylphenyl)-1,3-dioxolane
https://huagongshe.com/reaction/250522
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | p-METHYLACETOPHENONE | HCID 8500 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methyl-2-(4-methylphenyl)-1,3-dioxolane | HCID 2755469 | 79.1% |
Reaction Steps
A mixture of 4-methylacetophenone (1.00 g, 7.45 mmol), p-toluenesulfonic acid (133 mg, 0.745 mmol) and ethylene glycol (1.20 mL, 22.4 mmol) in dry toluene (20 mL) was heated at reflux with a Dean-Stark apparatus under nitrogen for 24 h. The mixture was allowed to cool to room temperature and the solvent was evaporated in vacuo. The residue was taken up in ether (20 mL) and the solution was washed with saturated sodium bicarbonate solution (2×10 mL) and brine (1×10 mL), then dried (Na2SO4) and concentrated under reduced pressure. Flash column chromatography of the residue, eluting with 37% aqueous ammonia:ether:hexane (0.02:1:6) afforded 2-methyl-2-(4-methylphenyl)-1,3-dioxolane (23) as a colourless oil (1.05 g, 59%). 1H nmr (200 MHz, CDCl3) 1.65 (s, 3H, CH3), 2.35 (s, 3H, ArCH3), 3.74-3.86 (m, 2H, OCH2), 3.94-4.06 (m, 2H, OCH2), 7.15 (d, J=8.2 Hz, 2H, 2×ArH), 7.37 (d, J=8.2 Hz, 2H, 2×ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863313B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-125d60b86bf04bc18b8c7532c6023856 |
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| Source note | uspto-grants-2011_01 |
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