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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23209Generated: October 25, 2026

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

https://huagongshe.com/reaction/23209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
ReactantMethyl 4-Boc-piperazine-2-acetateHCID 2756816—
SolventTetrahydrofuranHCID 8028—
Product1-Fmoc-4-Boc-Piperazine-2-acetic acidHCID 275679691.7%

Reaction Steps

A portion (5.2 g; 20 mmol) of the methyl 4-Boc-piperazine-2-acetate product from the previous step was combined with 60 mL of THF and 60 mL of 1 N NaOH (aqueous) and stirred at room temperature for 6 hours to saponify the methyl ester. The reaction was cooled to 0° C., adjusted to pH 9-10 with 10% HCl(aqueous), and 5.2 g (20 mmol) of FMOC-Cl was added. The reaction was stirred at room temperature for 6 hours, (adding 1 N NaOH (aqueous) to maintain pH 9-10) 1 hour, then acidified with 10% HCl to pH=1. The reaction was extracted twice, the combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give 8.56 g of the desired 4-Boc-1-Fmoc-piperazine-2-acetic acid (the compound of formula (XXIV)); 1H NMR (CDCl3) δ 1.4 (s,9), 2.5-3.0 (m,5) 3.9-4.2 (m,6), 4.5 (m,1), 7-25 (t,4), 7.32 (t,4), 7.48 (d,4), 7.75 (d, 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849739B2
Source datasetuspto-grants-2005_02
ORD IDord-1a9145d13d964fe58e1a408fd6fd08e6
Source noteuspto-grants-2005_02