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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489716Generated: October 27, 2026

Water → 4-Benzyloxy-3-cyclopentyloxybenzaldehyde

https://huagongshe.com/reaction/1489716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Benzyloxy-3-hydroxybenzaldehydeHCID 561369—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-Benzyloxy-3-cyclopentyloxybenzaldehydeHCID 21187899—

Reaction Steps

A stirred solution of 4-benzyloxy-3-hydroxybenzaldehyde (60.9 g; that is prepared as described in Reference Example 36) in dry dimethylformamide (270 mL) under nitrogen is treated portionwise with potassium carbonate (79.5 g). After stirring at room temperature for 45 minutes, it is treated with cyclopentyl bromide (34.3 mL), and the resulting suspension is heated at 60° C. for 8 hours. After cooling, the solution is evaporated to low bulk under reduced pressure, to give an oil. This oil is treated with water (250 mL) and diethyl ether (300 mL), and the aqueous layer is washed with further quantities of diethyl ether (2×50 mL). The combined ethereal extracts are washed with brine (1×50 mL) and with water (3×50 mL), dried over magnesium sulfate and evaporated. The resulting residue is crystallized from methanol, to give 4-benzyloxy-3-cyclopentyloxybenzaldehyde (79 g), m.p. 55°-56° C. [Elemental analysis: C,77.1; H,6.9%; calculated: C,77.0; H,6.8%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679696
Source datasetuspto-grants-1997_10
ORD IDord-51c0c0481bc5468291ecbb4180212a49
Source noteuspto-grants-1997_10