HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737250Generated: October 27, 2026
Acetic Anhydride → 2-[2-(2-Fluoro-phenyl)-vinyl]-3-o-tolyl-3H-pteridin-4-one
https://huagongshe.com/reaction/1737250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | 4(3H)-Pteridinone, 2-methyl-3-(o-tolyl)- | HCID 210797 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-[2-(2-Fluoro-phenyl)-vinyl]-3-o-tolyl-3H-pteridin-4-one | HCID 69709245 | 55.4% |
Reaction Steps
A mixture of fused zinc chloride (0.17 g, 1.25 mmol), dioxane (15 mL), 2-methyl-3-(2-methyl-phenyl)-3H-pteridin-4-one (0.174 g, 0.69 mmol, preparation 8), and 2-fluorobenzaldehyde (0.22 mL, 2.07 mmol), and acetic anhydride 0.195 mL, 2.07 mmol) was refluxed overnight. The reaction was cooled and concentrated. The residual material was partitioned between saturated aqueous sodium bicarbonate and methylene chloride. The layers were carefully shaken and separated. The organic layer was washed with brine, dried and concentrated. The residue was flash chromatographed on silica gel (0.75×4 inches) with elution proceeding as follows: 50% ethyl acetate/hexane (300 mL), forerun; 60% ethyl acetate/hexane (400 mL). 2-[2-(2-Fluoro-phenyl)-vinyl]-3-o-tolyl-3H-pteridin-4-one (0.137 g, 55%) was isolated as a yellow crystalline solid. A sample was recrystallized from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962457 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-2596b366804648f7bf2b5860aa278aac |
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| Source note | uspto-grants-1999_10 |
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