HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975619Generated: October 30, 2026
Benzaldehyde → 1,3-Dioxan-5-ol, 2-phenyl-
https://huagongshe.com/reaction/975619
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Glycerol | HCID 753 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | 1,3-Dioxan-5-ol, 2-phenyl- | HCID 74362 | — |
Reaction Steps
To a solution of benzaldehyde (150.0 g, 1.41 mol) in toluene, glycerol (160.0 g, 1.74 mol) was added followed by 4-methylbenzenesulfonic acid (1.0 g) and the mixture was vigorously stirred under reflux with a Dean-Stark water separator. The refluxing was continued until no more water separated in the condenser (6-8 h). The clear solution was treated with 4N NaOH until basic and the organic layer was washed with water (5×100 mL) followed by saturated sodium chloride solution and then dried over anhydrous sodium sulfate. Concentration of the organic layer resulted in an oil which was dissolved in hot isopropylether and then left in the freezer overnight. The colorless solid was filtered and washed with isopropylether to yield the title product as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05608110 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-5081947fd345463ca10300a2602e0ae7 |
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| Source note | uspto-grants-1997_03 |
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