HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50504Generated: October 26, 2026
3-Hydroxybenzaldehyde → 3-Isopropoxybenzaldehyde
https://huagongshe.com/reaction/50504
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 (7.86-46.2 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) 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 | US06710089B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-a85c68cf0b574b6abfd943208da65d44 |
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| Source note | uspto-grants-2004_03 |
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