HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093615Generated: November 1, 2026
4-Hydroxy-3-isopropenyl-5-nitrobenzonitrile → HCID 57917216, compound
https://huagongshe.com/reaction/2093615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxy-3-isopropenyl-5-nitrobenzonitrile | HCID 67140785 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57917216 | HCID 57917216 | — |
Reaction Steps
To a solution of 4-hydroxy-3-isopropenyl-5-nitrobenzonitrile (4.135 g, 20.25 mmol) in ethyl acetate (100 ml) was added 1.2 g of Pd/C. The resulting mixture was degassed and flushed with nitrogen, and then degassed and flushed with hydrogen using a double balloon. The reaction was stirred under hydrogen for 14 h, and then diluted with ethyl acetate, filtered through a pad of Celite and concentrated. The residue was purified by flash column chromatography using a Horizon Biotage, 65i Si column, eluting with 1 column volume of dichloromethane, followed by a linear gradient of ethyl acetate in dichloromethane from 0% to 50% over 10 column volume. It was then repurified by flash column chromatography using a Horizon Biotage, 65i Si column, eluting with 1 column volume of 5% ethyl acetate in hexanes, followed by a linear gradient of ethyl acetate in hexanes from 5% to 100% over 10 column volumes to afford the title compound. Mass spectrum (ESI) 177.4 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445480B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-ac7ba380441b49a7be46199332221d5b |
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| Source note | uspto-grants-2013_05 |
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