HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892256Generated: October 29, 2026
Potassium Iodide → 2-Methyl-4-[(prop-2-en-1-yl)oxy]benzaldehyde
https://huagongshe.com/reaction/892256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxy-2-methylbenzaldehyde | HCID 458185 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 2-Methyl-4-[(prop-2-en-1-yl)oxy]benzaldehyde | HCID 22242092 | 98% |
Reaction Steps
31.7 g (229 mmol) potassium carbonate and 9.51 g (57.3 mmol) potassium iodide were given to a solution of 15.6 g (115 mmol) 4-hydroxy-2-methyl-benzaldehyde and 55.4 g (458 mmol) allyl bromide in 500 ml 2-butanone and stirred for 16 h at 65° C. Solvents were distilled off and the residue distributed between ethyl acetate and 1 N sodium hydroxide. The organic layer was separated and the aqueous solution extracted once with ethyl acetate. The combined organic phases were dried and evaporated to give 19.8 g (98%) of 4-allyloxy-2-methyl-benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005526B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-18bf9a3d06064dd9baa6dd02eb02cf3b |
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| Source note | uspto-grants-2006_02 |
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