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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992269Generated: October 30, 2026

Water → (R,E)-N-(1-(5-bromo-2,4-difluorophenyl)ethylidene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1992269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
Reactant1-(5-Bromo-2,4-difluorophenyl)ethan-1-oneHCID 20785359—
SolventTetrahydrofuranHCID 8028—
Product(R,E)-N-(1-(5-bromo-2,4-difluorophenyl)ethylidene)-2-methylpropane-2-sulfinamideHCID 8663561281%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 1-(5-bromo-2,4-difluoro-phenyl)-ethanone (19 g, 64.7 mmoles, 1 equiv.) and (R)-2-methyl-propane-2-sulfinic acid amide (10.2 g, 84.1 mmoles, 0.76 equiv) in THF (0.3 M, 215 mL) is added Ti(OEt)4 (29.5 g, 129 mmoles, 2.0 equiv) in a single portion at ambient temperature. The reaction is heated to 70° C. and allowed to stir 18 h. The reaction is cooled to ambient temperature, and poured into water. The resulting suspension is filtered through a pad of diatomaceous earth and washed with ethyl acetate. The filtrate is collected and extracted with ethyl acetate. The organic layers are combined, dried over sodium sulfate, filtered, and concentrated under reduced pressure to give a residue. The residue is purified by silica gel chromatography, eluting with a linear gradient of hexane to hexane:ethyl acetate (3:1) over 20 minutes to give the title compound (81% yield): MS (m/z): 338, 340 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648983B2
Source datasetuspto-grants-2010_01
ORD IDord-0ba8c189cec94ce1af74de2431b16409
Source noteuspto-grants-2010_01