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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478619Generated: October 30, 2026

Sodium Hydroxide → 4-(4-{[(9H-fluoren-9-yl)methoxy]carbonyl}piperazin-1-yl)benzoic acid

https://huagongshe.com/reaction/478619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Piperazin-1-yl)benzoic acid hydrochlorideHCID 16876122—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-(4-{[(9H-fluoren-9-yl)methoxy]carbonyl}piperazin-1-yl)benzoic acidHCID 18002467—

Reaction Steps

4-Piperazin-1-yl-benzoic acid hydrochlorid (10.5 mmol) is dissolved in 15 ml Dioxan and 11.6 ml NaOH (2N) and cooled to 0° C. Simultaneously, FMOC-chloride (11.6 mmol) in dioxan (5 ml) and diisopropyl-ethylamine (11.6 mmol) in dioxan (5 ml) are added dropwise over 20 minutes at 0° C. and the mixture is stirred for 15 minutes and is then allowed to warm up to rt and is stirred over night. The mixture is diluted with water (50 ml) and extracted 2 times with diethylether. The water phase is acidified with aqueous HCl (4N) at 0-4° C. and the solid material formed is filtered off, washed with water and dried (vacuum). A white powder with Rf=0.2 (CH2Cl2/MeOH =95:5) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642239B2
Source datasetuspto-grants-2003_11
ORD IDord-00024c4d1a1e472783902e7e88893b42
Source noteuspto-grants-2003_11