HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262946Generated: November 1, 2026
Ethylene Glycol → 2-Phenyl-2-(2-thienyl)-1,3-dioxolane
https://huagongshe.com/reaction/1262946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2-Benzoylthiophene | HCID 67262 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Product | 2-Phenyl-2-(2-thienyl)-1,3-dioxolane | HCID 12962673 | — |
Reaction Steps
2-Benzoylthiophene (19 g., 0.1 mole), ethylene glycol (11 ml., 0.2 mole), toluene (150 ml.) and p-toluenesulfonic acid (about 0.2 g.) were combined and refluxed for 6 hours. By-product water was collected in a Dean-Stark trap. Tlc (1:8 ethyl acetate:hexane) indicated reaction to be about 40% complete. More ethylene glycol (30 ml.) was added and reflux continued for 35 hours. Reaction was still incomplete. The reaction mixture was diluted with 200 ml. of ether, washed twice with 150 ml. portions of water and concentrated to dryness. The residue was chromatographed on about 500 ml. of silica gel, with 1:8 ethyl acetate:hexane as eluant, monitored by tlc. Faster moving, product containing fractions were combined and evaporated to yield 2-phenyl-2-(2-thienyl)-1,3-dioxolane [8 g., oil, Rf 0.6 (1:8 ethyl acetate:hexane)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04454320 |
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| Source dataset | uspto-grants-1984_06 |
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| ORD ID | ord-436da4dd285d4a1aae632fa3b7699d33 |
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| Source note | uspto-grants-1984_06 |
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