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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482562Generated: October 31, 2026

4-Piperidinecarboxylic acid → 1-{[(9H-Fluoren-9-yl)methoxy]carbonyl}piperidine-4-carboxylic acid

https://huagongshe.com/reaction/482562

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinecarboxylic acidHCID 3773—
ReactantSodium carbonate dioxaneHCID 67151127—
Reactant(9H-fluoren-9-yl)methyl-2,5-dioxopyrrolidin-1-yl carbonateHCID 71304114—
Product1-{[(9H-Fluoren-9-yl)methoxy]carbonyl}piperidine-4-carboxylic acidHCID 273649095%

Reaction Steps

To a solution of 10.0 g (77.4 mmol) of isonipecotic acid (Aldrich) in 1N sodium carbonate/dioxane (1:1) at 0° C., was added 21.1 g (77.4 mmol) of 9-fluorenylmethylsuccinimidyl carbonate, portionwise. After 14 h, the dioxane was removed in vacuo, and the suspension diluted with 1200 mL of water. After extraction with 2 portions of ether (discarded), the aqueous solution was cooled in an ice bath and acidified to pH 3 with concentrated hydrochloric acid. The slurry was extracted twice with ethyl acetate and the combined organics washed with water, brine, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated to 500 mL, diluted with 700 mL of hexane, and placed in a refrigerator overnight. The product was collected on a filter and dried in vacuo to give 25.8 g (95%) of N-FMOC-isonipecotic acid as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798337
Source datasetuspto-grants-1998_08
ORD IDord-8dc084a657f044c5a9baea114759abde
Source noteuspto-grants-1998_08