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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | 6-bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-one | HCID 58424147 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(6-Bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-ylidene)-2-methylpropane-2-sulfinamide | HCID 67979529 | 90.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08865911B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-cc58bece168d475c913e6313ecab6e6d |
|---|
| Source note | uspto-grants-2014_10 |
|---|