HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-Methyl-propane-2-sulfonic acid 4-bromo-3-fluoro-benzylideneamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Bromo-3-fluorobenzaldehyde | HCID 2783411 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Methyl-propane-2-sulfonic acid 4-bromo-3-fluoro-benzylideneamide | HCID 86688556 | — |
Reaction Steps
11.1 g (91.0 mmol) 2-Methyl-2-propanesulfinamide are added to 16.5 g (76.0 mmol) 4-bromo-3-fluoro-benzaldehyde and 34.6 g (152 mmol) titanium(IV) ethoxide in 100 mL THF. Stirring is continued for 1.5 h at 50° C. After that time, the mixture is poured into brine. The mixture is filtered over celite and the filtrate is transferred to a separation funnel. The organic layer is separated, dried over magnesium sulphate and the solvent is removed by evaporation. The residue is purified by column chromatography (silica gel; gradient hexane/EtOAc 1:0→3:2) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765959B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-dc4432da03e244d5a32238de584a6647 |
| Source note | uspto-grants-2014_07 |