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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805922Generated: October 30, 2026

Isopropyl iodide → 4-(Benzyloxy)-2-isopropoxybenzaldehyde

https://huagongshe.com/reaction/1805922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Benzyloxy-2-hydroxybenzaldehydeHCID 561235—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-2-isopropoxybenzaldehydeHCID 10635744—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354454B2
Source datasetuspto-grants-2013_01
ORD IDord-6d1ffc315c6a4d248a1731c38bf7273d
Source noteuspto-grants-2013_01