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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627280Generated: October 30, 2026

2-((Tert-butyldimethylsilyl)oxy)acetaldehyde → (NE,S)-N-[2-[tert-butyl(dimethyl)silyl]oxyethylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/627280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((Tert-butyldimethylsilyl)oxy)acetaldehydeHCID 4187788—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
CatalystCopper SulfateHCID 24462—
SolventDichloromethaneHCID 6344—
Product(NE,S)-N-[2-[tert-butyl(dimethyl)silyl]oxyethylidene]-2-methylpropane-2-sulfinamideHCID 1600702361.7%

Reaction Steps

To a solution of 2-((tert-butyldimethylsilyl)oxy)acetaldehyde (Aldrich, 15 g, 86.05 mmol) in DCM (200 mL) at room temperature was added copper(II) sulfate (41.2 g, 258.16 mmol) and (S)-2-methylpropane-2-sulfinamide (Aldrich, 15.64 g, 129.08 mmol). The reaction mixture was stirred overnight at room temperature, then filtered through celite, washed with DCM and concentrated to afford an oil. Silica gel chromatography (0%-25% ethyl acetate/hexanes) afforded the title compound (14.73 g, 61.7%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309245B2
Source datasetuspto-grants-2016_04
ORD IDord-dbb08ed2d4554e48963ae006dee0bb71
Source noteuspto-grants-2016_04