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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277088Generated: October 27, 2026

Sodium Carbonate → (S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid

https://huagongshe.com/reaction/2277088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
Reactant(S)-4-N-Boc-piperazine-2-carboxylic acidHCID 1501850—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acidHCID 712830444.3%

Reaction Steps

To a stirred mixture of (S)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid (1.0 g, 4.34 mmol) and Na2CO3 (0.90 g, 10.80 mmol) in water (10 mL) was added solution of FMOC-Cl (1.23 g, 4.77 mmol) in 1,4-dioxane (10 mL) dropwise at 0° C. The reaction mixture was stirred at room temperature for 16 h then diluted with water (50 mL) and washed with MTBE (25 mL). The aqueous layer was acidified with 1N aqueous HCl (10 mL) to pH 2 and extracted with EtOAc (3×50 mL). The combined organic extracts were washed with brine solution (50 mL), dried over anhydrous Na2SO4, filtered and concentrated to afford the title compound (0.87 g) as an off-white solid. The crude product was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133147B2
Source datasetuspto-grants-2015_09
ORD IDord-58ff00aa787c42c2ab8096240564f92b
Source noteuspto-grants-2015_09