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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596003Generated: October 30, 2026

tert-Butylsulfinamide, (S)-(-)- → HCID 118045320, compound

https://huagongshe.com/reaction/596003

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
Reactant3-Bromo-5-fluorobenzaldehydeHCID 21986246—
CatalystCopper SulfateHCID 24462—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 118045320HCID 11804532099.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-bromo-5-fluorobenzaldehyde (5 g, 24.63 mmol) and (S)-2-methylpropane-2-sulfinamide (3.28 g, 27.1 mmol) in DCE (82 mL) was added copper(II) sulfate (anhydrous) (7.86 g, 49.3 mmol). The suspension was stirred under nitrogen at 60° C. overnight. The reaction mixture was cooled down, filtered through a plug of celite, and rinsed with DCM. The filtrate was concentrated to yield the crude product. The crude product was purified by flash chromatograph eluting with 0-30% EtOAc in heptane to yield the product (S,E)-N-(3-bromo-5-fluorobenzylidene)-2-methylpropane-2-sulfinamide (7.5 g, 24.49 mmol, 99% yield) as a light yellow color oil. LCMS (m/z): 306.1/308.1 (MH+), 1.04 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-51693e601ff34f6eb4acbfbcc2155695
Source noteuspto-grants-2016_01