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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770966Generated: 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/1770966

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 numberUS09248129B2
Source datasetuspto-grants-2016_02
ORD IDord-2e5b344b90b149e3a1a98efd50b7817a
Source noteuspto-grants-2016_02