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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936598Generated: November 1, 2026

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

https://huagongshe.com/reaction/1936598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
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 triethyl 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 numberUS06391877B1
Source datasetuspto-grants-2002_05
ORD IDord-06c95ac8cb7a48639501777c227ab2a3
Source noteuspto-grants-2002_05