Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480371Generated: November 1, 2026

Trifluoroacetic acid → 3,5-Dichlorobenzyl 4-(aminomethyl)-2-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1480371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3,5-Dichlorobenzyl 4-(((tert-butoxycarbonyl)amino)methyl)-2-methylpiperidine-1-carboxylateHCID 86722628—
SolventDichloromethaneHCID 6344—
Product3,5-Dichlorobenzyl 4-(aminomethyl)-2-methylpiperidine-1-carboxylateHCID 86722629—

Reaction Steps

A mixture comprising of 3,5-dichlorobenzyl 4-(((tert-butoxycarbonyl)amino)methyl)-2-methylpiperidine-1-carboxylate (step 3) (970 mg, 2.249 mmol) and trifluoroacetic acid (173 μl, 2.249 mmol) in DCM (7.5 ml) was left stirring at room temperature 18 hours. The resulting mixture was loaded on to a 10 g Isolute® SCX-2 cartridge and washed with MeOH. The product was eluted with 2M ammonia in MeOH and the product fractions were concentrated under reduced pressure to afford the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409895B2
Source datasetuspto-grants-2016_08
ORD IDord-a2e0a33bd73d473f8f69c2c74e52e146
Source noteuspto-grants-2016_08