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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525263Generated: November 2, 2026

1,4-Dibromobenzene → (R)-N-((R)-(4-bromophenyl)(2,4-difluorophenyl)methyl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1525263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
Reactant(NE,R)-N-[(2,4-difluorophenyl)methylidene]-2-methylpropane-2-sulfinamideHCID 88931146—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(R)-N-((R)-(4-bromophenyl)(2,4-difluorophenyl)methyl)-2-methylpropane-2-sulfinamideHCID 8946257322%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1,4-dibromobenzene (9.6 g, 40.77 mmol) was dissolved in THF (150 ml) and cooled to −78° C. under nitrogen. Then n-BuLi (16.3 ml, 40.77 mmol) was added dropwise below −60° C. After addition, the mixture was stirred at −78° C. for additional 1 h and then (R,E)-N-(2,4-difluorobenzylidene)-2-methylpropane-2-sulfinamide, 20-b, (10 g, 40.77 mmol) in anhydrous THF was added dropwise below −60° C. Then the mixture was allowed to stir at room temperature for 6 h. The mixture was quenched with saturated NH4Cl followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated under vacuum. The residue was purified by column chromatography (petroleum ether/ethyl acetate=4/1) to provide the product, 20-c, (3.6 g, 22%). HPLC indicated that the no obvious diastereomer was observed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079930B2
Source datasetuspto-grants-2015_07
ORD IDord-cc59571dc43b4ee58d9a2529bab6f998
Source noteuspto-grants-2015_07