HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopropyl methyl ketone → (NE)-N-(1-cyclopropylethylidene)-2-methylpropane-2-sulfinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopropyl methyl ketone | HCID 13004 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (NE)-N-(1-cyclopropylethylidene)-2-methylpropane-2-sulfinamide | HCID 89421056 | 27% |
Reaction Steps
A mixture of 1-cyclopropylethanone (1 g, 12 mmol), 2-methylpropane-2-sulfinamide (1.7 g, 14 mmol), Ti(OEt)4 (5.5 g, 24 mmol) in 10 mL of THF was heated at reflux with stirring overnight. The mixture was cooled to room temperature, solvent was removed under reduced pressure and the crude residue was purified by column chromatography (silica gel, 200-300 mesh, petroleum ether and ethyl acetate (3:1, v/v) to give (E)-N-(1-cyclopropylethylidene)-2-methylpropane-2-sulfinamide (0.6 g, 27%) as clear oil. MS: (M+H)+=188.2; 1H NMR (300 MHz, CDCl3): δ 2.36 (s, 3H), 1.69 (m, 1H), 1.18 (s, 9H), 1.07-0.89 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658646B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-6f96dc3d5ef041cd9850b2d5db0c244c |
| Source note | uspto-grants-2014_02 |