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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110033Generated: November 1, 2026

1-Boc-4-(aminomethyl)piperidine → N-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/2110033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
SolventTetrahydrofuranHCID 8028—
ProductN-(tert-butoxycarbonyl)piperidineHCID 7010304—

Reaction Steps

After dissolving 1-Boc-4-aminomethylpiperidine (2140 mg, 10 mmol) in tetrahydrofuran (25 ml), FmocNCS (3091 mg, 11 mmol) was added and the mixture was stirred at room temperature overnight. Upon completion of the reaction, the reaction mixture was concentrated, and then purified by silica gel column chromatography (hexane/ethyl acetate=85/15→4/1) to obtain [({[fluoren-9-ylmethoxy]carbonylamino}thioxomethyl)amino]methyl]piperidinecarboxylic acid tert-butyl ester. The compound was identified by LC-MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517875B2
Source datasetuspto-grants-2009_04
ORD IDord-9a00774b223f47478b619ebb66da36ea
Source noteuspto-grants-2009_04