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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336828Generated: October 29, 2026

4-Hydroxybenzaldehyde → HCID 86671378, compound

https://huagongshe.com/reaction/336828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantTriphenylphosphineHCID 11776—
Reactant1-Boc-4-(3-hydroxypropyl)piperazineHCID 16217800—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86671378HCID 8667137881.2%

Reaction Steps

To 0.5 g (2.05 mmol) of tert-butyl 4-(3-hydroxypropyl)piperazine-1-carboxylate, 0.3 g (2.46 mmol) of 4-hydroxybenzaldehyde and 1 g (3.07 mmol) of resin-supported triphenyl-phosphine (3 mmol/g of resin) diluted in 14.5 ml of anhydrous tetrahydrofuran, is added dropwise at 0° C. under argon 0.614 ml (3.07 mmol) of diisopropyldiazene-1,2-dicarboxylate. The reaction mixture is stirred at room temperature for 20 h. The solid is filtered then rinsed in dichloromethane. The filtrate is concentrated and diluted in a sodium hydroxide solution (1M) and the product is extracted several times with ethyl acetate. The organic phases are combined, dried over magnesium sulfate, and concentrated. The residue is purified by chromatography on silica (cyclohexane/ethyl acetate eluent: 4:6 to 100% ethyl acetate) to yield 0.58 g of tert-butyl 4-(3-(4-formylphenoxy)propyl)piperazine-1-carboxylate in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889711B2
Source datasetuspto-grants-2014_11
ORD IDord-e604bae373f4433b95b4ee70a0f7029a
Source noteuspto-grants-2014_11