HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56464Generated: October 29, 2026
Ethylene Glycol → 2-(6-Fluoro-3',5'-dimethoxy-4-nitrobiphenyl-3-yl)-1,3-dioxolane
https://huagongshe.com/reaction/56464
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 6-Fluoro-3',5'-dimethoxy-4-nitrobiphenyl-3-carbaldehyde | HCID 118036143 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(6-Fluoro-3',5'-dimethoxy-4-nitrobiphenyl-3-yl)-1,3-dioxolane | HCID 118036540 | 89% |
Reaction Steps
A mixture of 6-fluoro-3′,5′-dimethoxy-4-nitrobiphenyl-3-carbaldehyde (1.7 g, 5.6 mmol) and 4-toluenesulfonic acid (95.8 mg, 0.6 mmol) in 1,2-ethanediol (4.3 mL) and toluene (60 mL) was heated at 130° C. for 3 hours. After that, the reaction mixture was cooled to room temperature, diluted with ethyl acetate (100 mL), and washed by water (100 mL*3) and brine (100 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography (petroleum ether/ethyl acetate=8/1 to 5/1) to afford the title compound (1.8 g, 89%) as a yellow solid. MS (ES+) C17H16FNO6 requires: 349, found: 350 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434700B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-c6f276dd4f824154ad8a2db40e6ab5e4 |
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| Source note | uspto-grants-2016_09 |
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