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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624273Generated: November 1, 2026

1,4-Dibromobenzene → N-(3-(4-bromophenyl)oxetan-3-yl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/624273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamideHCID 46839995—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-(4-bromophenyl)oxetan-3-yl)-2-methylpropane-2-sulfinamideHCID 67067894—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a 50 mL round-bottomed flask was added 1,4-dibromobenzene (2.85 g, 12.07 mmol) in tetrahydrofuran (40.2 ml). The solution was cooled to −78° C. and n-butyl lithium (4.51 ml, 11.26 mmol) was added dropwise. The mixture was stirred for 1 hour at −78° C. 2-methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide (1.41 g, 8.05 mmol) was added as a tetrahydrofuran solution (ca 1 ml) and the reaction was stirred for 10 minutes and warmed to room temperature. Saturated ammonium chloride was added followed by water and dichloromethane. The aqueous layer was extracted twice with dichloromethane and the combined organics were dried with magnesium sulfate, filtered and concentrated under vacuum. The residue was purified by regular phase, flash column chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302989B2
Source datasetuspto-grants-2016_04
ORD IDord-da0af6dc42114bf2a8514e585f285db3
Source noteuspto-grants-2016_04