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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741387Generated: October 31, 2026

tert-Butanol → 2-((1S)-1,2-dihydroxyethyl)-4,5-diphenyloxazole

https://huagongshe.com/reaction/1741387

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantSodium SulfiteHCID 24437—
ReactantMethanesulfonamideHCID 72879—
Reactant2-Vinyl-4,5-diphenyloxazoleHCID 10890232—
Reactant1,4-Bis(dihydroquinidine)phthalazineHCID 11217202—
SolventWaterHCID 962—
Product2-((1S)-1,2-dihydroxyethyl)-4,5-diphenyloxazoleHCID 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). MS (m/z): 282 (M+ +1) IR (Neat): 3400 cm-1NMR (CDCl3, δ): 4.03 (1H, d, J=4.6 Hz), 4.90 (1H, t, J=4.6 Hz), 7.2-7.6 (10H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972965
Source datasetuspto-grants-1999_10
ORD IDord-7eb5a657be424393a1fb816cec409f8c
Source noteuspto-grants-1999_10