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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245898Generated: October 30, 2026

Tert-Butanesulfinamide → 2-methyl-N-[(1E)-1,3-oxazol-4-ylmethylidene]propane-2-sulfinamide

https://huagongshe.com/reaction/245898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButanesulfinamideHCID 3382465—
Reactant4-OxazolecarboxaldehydeHCID 14281432—
CatalystTitanium tetraethoxideHCID 76524—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-methyl-N-[(1E)-1,3-oxazol-4-ylmethylidene]propane-2-sulfinamideHCID 8942098989.2%

Reaction Steps

In a round-bottomed flask, oxazole-4-carbaldehyde (300 mg, 3.09 mmol) was dissolved in THF (7 ml) and 2-methylpropane-2-sulfinamide (450 mg, 3.71 mmol) and titanium(IV) ethoxide (1.3 ml, 6.18 mmol) were added. The reaction mixture was stirred at room temperature overnight then slowly quenched by dropwise addition of brine (2 ml) which resulted in the formation of a thick light yellow precipitate. The reaction mixture was diluted with ethyl acetate and stirred vigorously at room temperature for 30 min. The suspension was filtered over Celite and rinsed with ethyl acetate. The filtrate was concentrated and the residue was chromatographed over silica gel with EtOAc/hexanes (gradient 0-40% EtOAc) to afford 552 mg (89%) of 2-methyl-propane-2-sulfinic acid 1-oxazol-4-yl-meth-(E)-ylideneamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-9530f0ef6728462ebcaeec952ed721dc
Source noteuspto-grants-2014_02