HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791060Generated: November 4, 2026
Water → 5-Acetyl-2-{[2-(iodomethyl)-2-propenyl]oxy}benzaldehyde
https://huagongshe.com/reaction/1791060
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 5-Acetyl-2-{[2-(chloromethyl)-2-propenyl]oxy}benzaldehyde | HCID 22042271 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-Acetyl-2-{[2-(iodomethyl)-2-propenyl]oxy}benzaldehyde | HCID 22042281 | 100.1% |
Reaction Steps
531 mg (3.54 mmol) of sodium iodide are added to 894 mg (3.54 mmol) of 5-acetyl-2-{[2-(chloromethyl)-2-propenyl]oxy}benzaldehyde in solution in 10 ml of distilled acetone. The medium is brought to reflux and is stirred for 5 hours. Water is added and then the solution is concentrated. After the addition of water and dichloromethane, the phases are separated by settling and then the aqueous phase is extracted with dichloromethane. The combined organic phases are washed, dried and then concentrated under vacuum to give 1.22 g (100%) of 5-acetyl-2-{[2-(iodomethyl)-2-propenyl]oxy}benzaldehyde in the form of a white solid which turns yellow in air; 1H NMR (300 MHz, CDCl3): 10.46 (s, 1H), 8.34 (d, J=2.4 Hz, 1H), 8.15 (dd, J=2.4 Hz and 8.7 Hz, 1H), 7.08 (d, J=8.7 Hz, 1H), 5.52 and 5.32 (2s, 2H), 4.86 (s, 2H), 4.01 (s, 2H), 2.54 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071340B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-74898563749d45e290e940e012a4e69f |
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| Source note | uspto-grants-2006_07 |
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