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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475518Generated: November 1, 2026

4-Hydroxybenzaldehyde → HCID 21703917, compound

https://huagongshe.com/reaction/475518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantIsopropylethanediolHCID 7996—
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
Solventethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ProductHCID 21703917HCID 2170391782%

Reaction Steps

To a solution of 2-isopropoxyethanol (600 mg, 5.76 mmol), p-hydroxybenzaldehyde (0.78 g, 6.34 mM) and triphenylphosphine in THF (20 ml) (1.6 g, 6.1 mmol), diethyl azodicarboxylate (40% in toluene) was added at 0° C. over 10 minutes while stirring. Then, the mixture was stirred at room temperature for 18 hours until the initial reaction product of 2-isopropoxyethanol and p-hydroxybenzaldehyde disappeared. The resulting solution was concentrated and purified by silica gel chromatography (hexane:ethylacetate=5:1) to obtain 4-(2-isopropoxyethoxy)benzaldehyde as yellow oil (0.98 g, yield: 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637558B2
Source datasetuspto-grants-2014_01
ORD IDord-e5566eeb670641dfad8a422c6064d339
Source noteuspto-grants-2014_01