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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253005Generated: October 25, 2026

Triethylamine → (S)-N-(1-Hydroxybutan-2-yl)-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/253005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Nitrobenzenesulfonyl chlorideHCID 15540—
Reactant2-Amino-1-butanol, (+)-HCID 120084—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
Product(S)-N-(1-Hydroxybutan-2-yl)-2-nitrobenzenesulfonamideHCID 6686149699.1%

Reaction Steps

Triethylamine (0.94 ml, 6.74 mmol) was added to a solution of 400 mg (4.49 mmol) of (S)-2-aminobutan-1-ol in tetrahydrofuran (5 ml), and the mixture was stirred at room temperature for 10 min. 2-Nitrobenzenesulfonyl chloride (995.1 mg, 4.49 mmol) was added to the solution, and the mixture was stirred at room temperature for 15 min. A saturated aqueous sodium hydrogencarbonate solution was added thereto to stop the reaction, and the reaction solution was then extracted with ethyl acetate, was dried over anhydrous sodium sulfate, and was filtered. The filtrate was concentrated under the reduced pressure, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=2:1) to give 1.22 g (yield 99%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07871982B2
Source datasetuspto-grants-2011_01
ORD IDord-561b8a09e87945bf98599213f9276bfa
Source noteuspto-grants-2011_01