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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30186Generated: October 26, 2026

Hydrochloric Acid → 1-Fmoc-4-Boc-Piperazine-2-acetic acid

https://huagongshe.com/reaction/30186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
ReactantMethyl 4-Boc-piperazine-2-acetateHCID 2756816—
SolventSodium HydroxideHCID 14798—
Product1-Fmoc-4-Boc-Piperazine-2-acetic acidHCID 2756796—

Reaction Conditions

Temperature5 °C

Reaction Steps

3-Methoxycarbonylmethylpiperazine-1-carboxylic acid tert-butyl ester (6.0 g) was dissolved in TBF (60 ml) and 1N sodium hydroxide solution (60 ml) and stirred at room temperature for 6 hours. The solution was then cooled to 5° C. and adjusted to pH 9-10 by the addition of 10% hydrochloric acid. Nα(9-Fluorenylmethoxycarbonyl chloride (6.05 g) was then added portionwise, maintaining the pH at 9-10 by the addition of 1N NaOH solution. The reaction mixture was stirred at 5° C. for 16 hours. The solution was then adjusted to pH 1 by the addition of 10% hydrochloric acid. The solution was extracted with ethyl acetate (×2), dried (MgSO4) and evaporated. The title compound was obtained as a white foam (9.96 g), mass spectrum (API+) 411 [(M-C4H8)H+], C26H30N2O6 requires 466.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423052B2
Source datasetuspto-grants-2008_09
ORD IDord-bd2c7ff1f3a949b6b56b20e3ea0f6d2b
Source noteuspto-grants-2008_09