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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57427Generated: October 26, 2026

Ethylacetate heptane → (R)-N-((S)-1-(4-bromo-2,5-difluorophenyl)ethyl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/57427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylacetate heptaneHCID 21899848—
Reactant(NE,R)-N-[(4-bromo-2,5-difluorophenyl)methylidene]-2-methylpropane-2-sulfinamideHCID 90413979—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product(R)-N-((S)-1-(4-bromo-2,5-difluorophenyl)ethyl)-2-methylpropane-2-sulfinamideHCID 9034755891%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (R,E)-N-(4-bromo-2,5-difluorobenzylidene)-2-methylpropane-2-sulfinamide (7.2 g, 22.2 mmol in CH2Cl2 (200 mL) cooled to 0° C. (water/ice bath) under nitrogen, was added 3M methyl magnesium bromide (29.6 mL, 89 mmol) in Et2O. Reaction mixture allowed to stir for 5 hours at 0° C. then quenched with the slow addition of a saturated solution of NH4Cl. Aqueous mixture adjusted to pH 8 with HCl (1 N) and extracted with DCM. Organic phases combined, washed with water, brine, dried (Na2SO4), filtered and concentrated onto silica gel. Silica gel column chromatography (EtOAc/Heptane 30 to 100%) provided (R)—N—((S)-1-(4-bromo-2,5-difluorophenyl)ethyl)-2-methylpropane-2-sulfinamide (6.86 g, 20.2 mmol, 91% yield) LCMS m/z 342.1 (M+H)+, Rt 0.96 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-fcf99e8a98824f6ab2a801c98bca4c2f
Source noteuspto-grants-2016_09