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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393047Generated: October 25, 2026

Hydrochloric Acid → 3-(9H-fluoren-9-ylmethoxycarbonylamino)cyclohexane-1-carboxylic Acid

https://huagongshe.com/reaction/393047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Aminocyclohexanecarboxylic acidHCID 544887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-(9H-fluoren-9-ylmethoxycarbonylamino)cyclohexane-1-carboxylic AcidHCID 426011057%

Reaction Steps

3-Aminocyclohexanecarboxylic acid (10 g, 70 mmol) was added to a solution of sodium hydrogen carbonate (7.6 g, 91 mmol) in water (100 mL). A solution of 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]oxy-2,5-pyrrolidinedione (Fmoc-OSu; 28.3 g, 84 mmol) in tetrahydrofuran (200 mL) was added. The solution was stirred at room temperature overnight and then poured into 3 M HCl (200 mL). The mixture was extracted with ethyl acetate (100 mL then 50 mL) and the combined organic layers were washed with saturated brine (3×100 mL), dried (Na2SO4), filtered, and concentrated to approximately 200 mL. Crystallization occurred on concentration. The mixture was allowed to stand overnight, then the solid was filtered off, washed with ethyl acetate and dried in a vacuum oven at 55° C. to give 3-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid (14.66, 57%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06803384B2
Source datasetuspto-grants-2004_10
ORD IDord-3fa3914117414d038e65cf407de2d41c
Source noteuspto-grants-2004_10