HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518847Generated: October 31, 2026
Isopropyl iodide → HCID 62116082, compound
https://huagongshe.com/reaction/518847
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Hydroxy-4-nitrobenzaldehyde | HCID 69712 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 62116082 | HCID 62116082 | — |
Reaction Steps
3.0 g of 3-hydroxy-4-nitrobenzaldehyde, 30 ml of acetonitrile, 5.9 g of caesium carbonate and 4.1 ml of 2-iodopropane are successively introduced into a three-necked round-bottomed flask under argon. The reaction mixture is heated at 70° C. for 17 h. After cooling to ambient temperature, the mixture is filtered through a sintered glass filter and the filtrate is concentrated to dryness under reduced pressure. The residue is taken up in a mixture of 50 ml of ethyl acetate and 15 ml of water, and then separated by settling out. The aqueous phase is separated and the organic phase is washed with 10 ml of water. The organic phase is then dried over magnesium sulfate and then concentrated to dryness under reduced pressure, so as to obtain 3.6 g of 3-isopropoxy-4-nitrobenzaldehyde in the form of a dark brown liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115140B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-f143b00ec639456d8f5cbda9500298b6 |
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| Source note | uspto-grants-2015_08 |
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