HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl mercaptan → 2-[2-Fluoro-6-(1,1-dimethylethylthio)phenyl]-4,4-dimethyl-2-oxazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl mercaptan | HCID 6387 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Oxazole, 2-(2,6-difluorophenyl)-4,5-dihydro-4,4-dimethyl- | HCID 10987554 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2-Fluoro-6-(1,1-dimethylethylthio)phenyl]-4,4-dimethyl-2-oxazoline | HCID 18630015 | 83% |
Reaction Steps
A mixture of 2-methyl-2-propanethiol (2.7 g, 30 mmol), the compound of example g (3.17 g, 15 mmol), and NaH (0.79 g, 33 mmol) in THF (100 mL) was stirred at RT for 1 d, then at reflux for 1 d. This was then quenched with sat aq NaHCO3 (50 mL) and extracted with EtOAc (3×50 mL). The combined organic extracts were dried (MgSO4), concentrated, ard purified by HPLC with 1:4 EtOAc/hexanes to afford 3.5 g of 2-[2-fluoro-6-(1,1-dimethylethylthio)phenyl]-4,4-dimethyl-2-oxazoline as a yellow oil, an 83% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998466 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-57caee1541fd498c8f1b8baa38f34227 |
| Source note | uspto-grants-1999_12 |