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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170046Generated: October 31, 2026

Sulfuric acid magnesium salt (1:1) → (R,E)-N-(2-((tert-butyldimethylsilyl)oxy)ethylidene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/2170046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant2-((Tert-butyldimethylsilyl)oxy)acetaldehydeHCID 4187788—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
SolventDichloromethaneHCID 6344—
Product(R,E)-N-(2-((tert-butyldimethylsilyl)oxy)ethylidene)-2-methylpropane-2-sulfinamideHCID 86644143—

Reaction Steps

(R)-(+)-2-methyl-2-propanesulfinamide (8.70 g, 71.8 mmol), pyridinium p-toluenesulfonate (0.902 g, 3.59 mmol) and MgSO4 (43.2 g, 359 mmol) was suspended in methylene chloride (25 mL). A solution of (tert-butyldimethylsilyloxy)acetaldehyde (25.0 g, 144 mmol) dissolved in methylene chloride (10 mL) was added drop wise at room temperature. The reaction was stirred at room temperature overnight. The mixture was evaporated to dryness. Flash chromatography (silica, EtOAc/heptanes 1:4) gave the title compound as an oil that slowly solidified upon standing (18.3 g, 92%) sufficiently pure for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050327B2
Source datasetuspto-grants-2015_06
ORD IDord-e4a281b9638f4cdd9caab4c8cd46f024
Source noteuspto-grants-2015_06