HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990549Generated: October 29, 2026
3-Hydroxybenzaldehyde → 3-Isopropoxybenzaldehyde
https://huagongshe.com/reaction/990549
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
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 (3×). The combined ether layer was washed with water, 2 M NaOH. again with water until clear (4×), 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) δ9.62 (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 | US06458852B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-a808df3e44c34dc791bf195fde675fa8 |
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| Source note | uspto-grants-2002_10 |
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