HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991345Generated: October 31, 2026
3-Hydroxybenzaldehyde → 3-Isopropoxybenzaldehyde
https://huagongshe.com/reaction/991345
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 3-Isopropoxybenzaldehyde | HCID 712914 | 67% |
Reaction Steps
EX-645A) 3-Hydroxybenzaldehyde (5.60 g, 45.9 mmol) and 2-iodopropane (7.86 g, 46.2 mmol) were dissolved in 50 mL of isopropanol. Potassium carbonate (20 g, 145 mmol) was added, and the mixture was heated to reflux for 8 h, at which time TLC analysis indicated that the reaction had gone to completion. Water was added to dissolve all solids, and the mixture was extracted with ether (3x). The combined ether layer was washed with water, 2 M NaOH, again with water until clear (4x), and finally with brine. The solution was dried over MgSO4, filtered, and evaporated to give 5.03 g (67%) of the desired 3-isopropoxybenzaldehyde product as a pale oil. 1H NMR (C6D6) δ 9.62 (s, 1H), 7.29 (s, 1H), 7.03 (m, 1H), 6.91 (t, 1H), 6.84 (m, 1H), 4.03 (septet, 1H), 0.96 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06462092B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-0e5684627b3747428380152ea872789a |
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| Source note | uspto-grants-2002_10 |
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