HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → 2-((1S)-1,2-dihydroxyethyl)-4,5-diphenyloxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 2-Vinyl-4,5-diphenyloxazole | HCID 10890232 | — |
| Reactant | 1,4-Bis(dihydroquinidine)phthalazine | HCID 11217202 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-((1S)-1,2-dihydroxyethyl)-4,5-diphenyloxazole | HCID 56982726 | — |
Reaction Steps
A solution of AD-mix-β (trade name, Aldrich) (114 g) in a mixture of t-butyl alcohol (400 ml) and water (400 ml) was stirred for 1 hour, and then methanesulfonamide (7.6 g) and 2-vinyl-4,5-diphenyloxazole (20 g) was added to the solution at 0° C. After being stirred for 8 hours at the same temperature, sodium sulfite (50 g) was added, and the mixture was stirred for 30 minutes. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with 1N-HCl solution, sat. NaHCO3, and brine, dried over MgSO4, and evaporated in vacuo. The residue was purified by trituration with hexane-ether to afford 2-((1S)-1,2-dihydroxyethyl)-4,5-diphenyloxazole (21 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06300344B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-8d279bcf916f4d24afaf1dea6c42ad33 |
| Source note | uspto-grants-2001_10 |