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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539361Generated: October 25, 2026

Tert-Butanesulfinamide → N-(6-Bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-ylidene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/539361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButanesulfinamideHCID 3382465—
Reactant6-bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-oneHCID 58424147—
CatalystTitanium tetraethoxideHCID 76524—
SolventWaterHCID 962—
Solvent2-MethyltetrahydrofuranHCID 7301—
SolventEthyl AcetateHCID 8857—
ProductN-(6-Bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-ylidene)-2-methylpropane-2-sulfinamideHCID 6797952990.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

6-Bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-one (Intermediate 27, 1.5 g, 4.82 mmol) and 2-methylpropane-2-sulfinamide (1.052 g, 8.68 mmol) were dissolved in dry 2-methyl-tetrahydrofuran (12 mL). Neat titanium ethoxide (1.788 mL, 8.68 mmol) was added. The resulting mixture was heated by MW at 130° C. for 60 min. The mixture was diluted with EtOAc (150 mL) and water (40 mL) was added dropwise during vigorous stirring of the reaction mixture. The stirring was continued for 15 min. The solid was decanted and the mixture filtered through a pad of diatomaceous earth. The organic layer was separated, dried over MgSO4 and vacuum filtered directly through a pad of silica (approx. 10 g) and concentrated in vacuo to give the title compound (1.8 g, 90% yield). MS (ES+) m/z 414 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865911B2
Source datasetuspto-grants-2014_10
ORD IDord-cc58bece168d475c913e6313ecab6e6d
Source noteuspto-grants-2014_10