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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606993Generated: October 29, 2026

(R)-2-Benzhydryloxirane → (2S)-1,1-diphenyl-pent-4-ene-2-ol

https://huagongshe.com/reaction/606993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-BenzhydryloxiraneHCID 11789056—
ReactantHCID 178418507HCID 178418507—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product(2S)-1,1-diphenyl-pent-4-ene-2-olHCID 1139077670.5%

Reaction Steps

(2R)-2-benzhydryl-oxirane (0.5 g, 2.38 mmol) 23a was dissolved in dry THF (5 ml) and was added into a dry THF solution at −78° C. containing CuI (0.045 g, 0.24 mmol) and vinylmagnesium bromide (5.95 ml of 1.0M solution in THF, 5.95 mmol). The reaction mixture was stirred and allowed to reach room temperature over a period of 2h, and then quenched with saturated NH4Cl solution. The aqueous phase was extracted with ethyl acetate (3×30 ml). The combined organic phase was washed with brine and dried over anhydrous Na2SO4. The solvent was removed and the residue was purified by flash chromatography on silica gel (Hexane/Ethyl Ether=4:1) to give 0.4 g (2S)-1,1-diphenyl-pent-4-ene-2-ol (70%, [α]D=(−)25, c=1, MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915433B2
Source datasetuspto-grants-2011_03
ORD IDord-97f420b978bd400da66a1de4670d2f68
Source noteuspto-grants-2011_03