HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254801Generated: October 30, 2026
p-Aminoacetophenone → HCID 58230610, compound
https://huagongshe.com/reaction/254801
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Aminoacetophenone | HCID 7468 | — |
| Reactant | Cyclopentadiene | HCID 7612 | — |
| Reactant | HCID 10900934 | HCID 10900934 | — |
| Catalyst | Scandium(III) triflate | HCID 2734571 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58230610 | HCID 58230610 | 97% |
Reaction Steps
A solution of the catalyst Sc(OTf)3 (0.032 g, 0.065 mmol, 10 mol %) in acetonitrile (0.2 mL) was added to the mixture of 6-trimethylsilanylethynyl-benzo[1,3]dioxole-5-carbaldehyde (0.160 g, 0.65 mmol), p-aminoacetophenone (0.0878 g, 0.65 mmol) and cyclopentadiene (0.214 g, 3.25 mmol) in acetonitrile (3 mL). The reaction was stirred at ambient temperature (˜23° C.) and the progress was monitored by thin layer chromatography. The reaction was complete after 2 hr. The reaction mixture was worked up by removal of solvent and other volatiles by evaporation under reduced pressure. The crude material was purified by preparative column chromatography using silica gel (SiO2) eluted with EtOAc/hexane (polar phase composition 8% EtOAc). The fractions containing pure product were evaporated in vacuo. The yield was 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875721B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-2c7d0522ddfd416d827b85f24fd1e849 |
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| Source note | uspto-grants-2011_01 |
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