Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | HCID 67979501 | HCID 67979501 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67979386 | HCID 67979386 | 69.3% |
Reaction Steps
6″-Bromodispiro[1,3-dioxolane-2,1′-cyclohexane-4′,2″-inden]-1″(3″H)-one (Intermediate 71, 320 mg, 0.95 mmol), 2-methylpropane-2-sulfinamide (173 mg, 1.42 mmol) and titanium ethoxide (0.391 mL, 1.90 mmol) were dissolved in 2-Me THF (5 mL) and heated to reflux overnight. The reaction was stopped and was left to cool down to r.t. EtOAc and water were added under stirring. The mixture was left to stand still for 2 h. The organic phase was collected by filtration, dried using a phase separator and concentrated in vacuo. The crude product was purified by flash chromatography using a gradient of 0-30% EtOAc in heptane to give the title compound (290 mg, 69% yield): 1 H NMR (500 MHz, CDCl3) δ ppm 1.35 (s, 9 H) 1.48-1.54 (m, 1 H) 1.61 (dd, 1 H) 1.67-1.77 (m, 2 H) 1.81-1.90 (m, 2 H) 2.10 (br. s., 2 H) 2.95-3.05 (m, 2 H) 3.95-4.02 (m, 4 H) 7.25 (s, 1 H) 7.60 (dd, 1 H) 8.62 (br. s., 1 H); MS (ES+) m/z 440.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865911B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-dc348ad247924e0081336e7217e57664 |
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| Source note | uspto-grants-2014_10 |
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