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 1d, then at reflux for 1d. 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, and 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 | US06028101 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-c1014414c52848b7831a3399f3fcf9ad |
| Source note | uspto-grants-2000_02 |