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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535146Generated: October 30, 2026

4-Nitrobenzenesulfonyl chloride → ethyl 2-{[(4-nitrophenyl)sulfonyl]amino}-4-(tetrahydro-4H-pyran-4-ylidene)butanoate

https://huagongshe.com/reaction/535146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
ReactantDiisopropylethylamineHCID 81531—
Reactantethyl 2-amino-4-(tetrahydro-4H-pyran-4-ylidene)butanoateHCID 58313060—
SolventDichloromethaneHCID 6344—
Productethyl 2-{[(4-nitrophenyl)sulfonyl]amino}-4-(tetrahydro-4H-pyran-4-ylidene)butanoateHCID 58313106—

Reaction Steps

To a solution of ethyl 2-amino-4-(tetrahydro-4H-pyran-4-ylidene)butanoate (163) (1.0 g, 4.7 mmol) in anhydrous dichloromethane (30 mL) was added Hunig's base (1.6 mL, 9.4 mmol) followed by 4-nitrobenzenesulfonyl chloride (1.14 g, 5.2 mmol) and the reaction stirred at room temperature under nitrogen for 2 h. The reaction was diluted with dichloromethane and washed with 0.1 N HCl, the organic layer was dried over MgSO4 and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 10-70% hexanes/EtOAc to afford the title compound as an off-white solid in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853416B2
Source datasetuspto-grants-2014_10
ORD IDord-f37fb00e5cbc48e58bd70642978897f2
Source noteuspto-grants-2014_10