HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351817Generated: October 26, 2026
4-Hydroxybenzaldehyde → 4-Isopropoxybenzaldehyde
https://huagongshe.com/reaction/351817
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Isopropoxybenzaldehyde | HCID 250077 | 77.3% |
Reaction Steps
To a solution of 2 g (16.38 mmol) of 4-hydroxybenzaldehyde in 100 mL of DMF, 2.72 g (19.69 mmol) of K2CO3, 2.74 g (16.52 mmol) of KI and 3.94 mL (39.38 mmol) of 2-iodopropane was added under argon. The mixture was stirred at 80° C. overnight, concentrated and the residue obtained was partitioned between CHCl3 and H2O. The phases were separated, the aqueous phase was extracted with CHCl3 and the combined organic phases were dried over MgSO4 and concentrated. The crude product obtained was purified by chromatography on silica gel using EtOAc/hexane mixtures of increasing polarity as eluent, to give 2.08 g of the title compound of the example as an oil (77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743816B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-894b4acbbcc04531b679f4df06420873 |
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| Source note | uspto-grants-2004_06 |
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