HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805922Generated: October 30, 2026
Isopropyl iodide → 4-(Benzyloxy)-2-isopropoxybenzaldehyde
https://huagongshe.com/reaction/1805922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzyloxy-2-hydroxybenzaldehyde | HCID 561235 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Benzyloxy)-2-isopropoxybenzaldehyde | HCID 10635744 | — |
Reaction Steps
K2CO3 (6.14 g, 44.4 mmol) and 2-iodopropane (1.28 mL, 12.76 mmol) were added successively to a stirred solution of 4-benzyloxy-2-hydroxybenzaldehyde (2.33 g, 10.21 mmol) in dry DMF (12.8 mL) at 25° C. under N2. The reaction was heated at 50° C. overnight. The reaction was diluted with water (50 mL) and extracted with Et2O (3×50 mL). The combined extracts were dried (MgSO4) and concentrated in vacuo to afford the crude product. This was azeotroped from toluene to afford 4-(benzyloxy)-2-isopropoxybenzaldehyde. LCMS calc.=293.1; found=292.9 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354454B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-6d1ffc315c6a4d248a1731c38bf7273d |
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| Source note | uspto-grants-2013_01 |
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