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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581951Generated: November 4, 2026

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

https://huagongshe.com/reaction/1581951

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 numberUS06734182B2
Source datasetuspto-grants-2004_05
ORD IDord-f9aa1e09d3da4c24b3cab615d9e4a42a
Source noteuspto-grants-2004_05