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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337198Generated: October 29, 2026

4-Nitrobenzenesulfonyl chloride → [1-(4-Nitro-benzenesulfonyl)-piperidin-4-yl]carbamic acid tert-butyl ester

https://huagongshe.com/reaction/337198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
SolventDichloromethaneHCID 6344—
Product[1-(4-Nitro-benzenesulfonyl)-piperidin-4-yl]carbamic acid tert-butyl esterHCID 7107953892.6%

Reaction Steps

Diisopropylethylamine (4.5 ml, 27.0 mmol) was added in one portion to a stirred solution of piperidin-4-yl-carbamic acid tert-butyl ester (5.0 g, 20.0 mmol) in DCM (40 ml) at room temperature. To this mixture was added 4-nitrophenyl sulfonyl chloride (6.0 g, 27.0 mmol) in one portion and the mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour. After this time the mixture was diluted with DCM (100 ml) and washed sequentially with HCl (1M solution, 50 ml), NaOH (1M solution, 50 ml) and brine (50 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated. The resulting solid was collected by filtration, dried with diethyl ether and dried under vacuum give the title compound (7.14 g, 74% yield) as a pale yellow solid. Tr=2.07 min m/z (ES+) (M+Na+) 408.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889716B2
Source datasetuspto-grants-2014_11
ORD IDord-664feb377bcf4560b78372af9dbb3df8
Source noteuspto-grants-2014_11