Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965125Generated: October 26, 2026

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

https://huagongshe.com/reaction/1965125

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 numberUS08415483B2
Source datasetuspto-grants-2013_04
ORD IDord-1e225fa75cbb45c5aa958e71fc50abf6
Source noteuspto-grants-2013_04