HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518882Generated: November 1, 2026
Isopropyl iodide → 7-Isopropoxy-3,4-dihydronaphthalen-1(2H)-one
https://huagongshe.com/reaction/518882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 7-hydroxy-3,4-dihydro-2H-naphthalen-1-one | HCID 571818 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Isopropoxy-3,4-dihydronaphthalen-1(2H)-one | HCID 14256760 | — |
Reaction Steps
A suspension of 2.0 g of 7-hydroxy-3,4-dihydronaphthalen-1(2H)-one, 4.04 g of caesium carbonate and 3.15 ml of 2-iodopropane in 23 ml of acetonitrile is heated for 1 hour at 80° C. The reaction medium is brought back to ambient temperature and then evaporated to dryness. The residue is taken up with 100 ml of water and 100 ml of ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and evaporated under reduced pressure, so as to obtain 2.24 g of 7-(propan-2-yloxy)-3,4-dihydronaphthalen-1(2H)-one in the form of an orangey-coloured oil.
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-848244ca0ede49a4b28ee9665ed1f324 |
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| Source note | uspto-grants-2015_08 |
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