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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322478Generated: October 27, 2026

2-Nitrobenzenesulfonyl chloride → tert-Butyl 6-{[(2-nitrophenyl)sulfonyl]amino}hexylcarbamate

https://huagongshe.com/reaction/322478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
Reactanttert-Butyl (6-aminohexyl)carbamate monohydrochlorideHCID 3017638—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 6-{[(2-nitrophenyl)sulfonyl]amino}hexylcarbamateHCID 5392129287.2%

Reaction Steps

To a stirred solution of N-Boc 1,6-diaminohexane hydrochloride (1.51 g, 6 mmol) and triethyle amine (1.31 g, 13 mmol) in 50 mL methylene chloride was added 2-Nitrobenzenesulfonyl chloride (1.326 g, 6 mmol). The reaction mixture was stirred for 6 h at room temperature, quenched with brine, and extracted with methylene chloride (2×50 mL). The organic layer was washed with brine (a saturated solution of sodium chloride in water, unless otherwise specified), dried over anhydrous sodium sulfate, and concentrated in vacuo to yield the titled compound as yellow oil (2.1 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211241B1
Source datasetuspto-grants-2001_04
ORD IDord-c9541adc391f44d994d0a3033ecf13ff
Source noteuspto-grants-2001_04