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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336832Generated: October 25, 2026

Water → Tert-butyl 4-(4-formyl-2-methoxyphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/336832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant4-Fluoro-3-methoxybenzaldehydeHCID 2737358—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 4-(4-formyl-2-methoxyphenyl)piperazine-1-carboxylateHCID 8667138051%

Reaction Conditions

Temperature90 °C

Reaction Steps

To 400 mg (2.60 mmol) of 4-fluoro-3-methoxybenzaldehyde diluted in 10 ml of dimethylsulfoxide are respectively added 483 mg (2.60 mmol) of tert-butyl piperazine-1-carboxylate, then 394 mg (2.85 mmol) of potassium carbonate. The solution is heated to 90° C. for 40 h, then water is added and the product is extracted several times with ethyl acetate. The organic phases are combined, dried over magnesium sulfate, and concentrated. The residue obtained is purified by chromatography on silica (cyclohexane/ethyl acetate eluent: 8:2) to yield 425 mg of tert-butyl 4-(4-formyl-2-methoxyphenyl)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-d758faf30d914d1d943e1c7686ed1efc
Source noteuspto-grants-2014_11