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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370749Generated: October 29, 2026

Ethyl Acetate → (NE,S)-N-[(3-fluoro-2-pyridinyl)methylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/2370749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-Fluoro-2-pyridinecarboxaldehydeHCID 11344017—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
CatalystCopper SulfateHCID 24462—
SolventDichloromethaneHCID 6344—
Product(NE,S)-N-[(3-fluoro-2-pyridinyl)methylidene]-2-methylpropane-2-sulfinamideHCID 89310556—

Reaction Steps

A mixture of 3-fluoropicolinaldehyde (300 g, 2400 mmol), copper sulfate (572 g, 3600 mmol) and (S)-2-methylpropane-2-sulfinamide (319 g, 2640 mmol) in DCM (3 L) in a 10 L 3-neck round bottom flask was stirred for 3 h at rt. The progress of the reaction was monitored by TLC (30% EtOAc in petroleum ether). After completion of reaction, the solid was filtered off and the filtrate was concentrated under vacuum. The initially obtained product was purified by column chromatography using silica (60-120 mesh) with 20% EtOAc in n-hexane as eluent to give the title compound sulfinamide as yellow oil. 1H-NMR (400 MHz, CDCl3): δ ppm 8.89 (s, 1H), 8.64 (s, 1H), 7.55 (t, J=8.4 Hz, 1H), 7.46 (d, J=3.6 Hz, 1H), 1.29 (s, 9H). MS (ESI pos. ion) m/z: 155.0 (M-O and t-Bu).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710043B2
Source datasetuspto-grants-2014_04
ORD IDord-a72ade74d60745dfb1a0ffa51870d2ec
Source noteuspto-grants-2014_04