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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442382Generated: October 26, 2026

4-Hydroxybenzaldehyde → 4-(2-Benzyloxycarbonyl-2-methylpropoxy)benzaldehyde

https://huagongshe.com/reaction/1442382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantBenzyl 3-hydroxy-2,2-dimethylpropanoateHCID 18922595—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Benzyloxycarbonyl-2-methylpropoxy)benzaldehydeHCID 2307785314%

Reaction Steps

To a solution of 4-hydroxybenzaldehyde (2.7 g), benzyl hydroxypivalate (4.7 g) and triphenylphosphine (6.4 g) in tetrahydrofuran (22 mL) was added diethyl azodicarboxylate (40% toluene solution, 11 mL), and the mixture was stirred at room temperature for 2 days. The reaction mixture was poured into water, and the resulting mixture was extracted with diethyl ether. The organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=6/1-4/1) to give the title compound (0.97 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655632B2
Source datasetuspto-grants-2010_02
ORD IDord-f288aa0b042348599b29e82c25c01935
Source noteuspto-grants-2010_02