Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptane | HCID 8900 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | 6-bromo-3,4-dihydro-2H-1-benzopyran-4-one | HCID 4197451 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67979564 | HCID 67979564 | 83% |
Reaction Steps
6-Bromochroman-4-one (5.0 g, 22 mmol) and 2-methylpropane-2-sulfinamide (2.6 g, 22 mmol) were dissolved in dry THF (80 mL). Titanium ethoxide (10 g, 44 mmol) was added. The resulting mixture was heated at 60° C. for 2 days. An additional portion of titanium ethoxide (1.0 g, 8.4 mmol) was added after 12 h. The mixture was mixed with heptane and evaporated onto silica gel. Flash chromatography on silica (0-50% EtOAc in heptane) gave the title compound (6.0 g, 83% yield). 1H NMR (500 MHz, CDCl3) δ ppm 1.34 (s, 9 H) 3.26-3.32 (m, 1 H) 3.47-3.54 (m, 1 H) 4.28-4.40 (m, 2 H) 6.83 (d, 1 H) 7.46 (dd, 1 H) 8.06 (d, 1 H); MS (ES+) m/z 330 [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-d686bc0d033a493ebbb2a913ed3faded |
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| Source note | uspto-grants-2014_10 |
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