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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025807Generated: November 1, 2026

Lithium borohydride → 2-{4-[1-(4-Iodophenyl)-1,2-dimethylpropyl]phenoxy}-2-pyridin-2-ylpropan-1-ol

https://huagongshe.com/reaction/1025807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantMethyl 2-{4-[1-(4-iodophenyl)-1,2-dimethylpropyl]phenoxy}-2-pyridin-2-ylpropanoateHCID 58381237—
SolventTetrahydrofuranHCID 8028—
Product2-{4-[1-(4-Iodophenyl)-1,2-dimethylpropyl]phenoxy}-2-pyridin-2-ylpropan-1-olHCID 58381243—

Reaction Steps

Lithium borohydride (1 equiv) is added to a stirred solution of 5d (1 equiv) in THF at room temperature. After completion of reaction, the reaction mixture is quenched with 2 N HCl, poured into saturated aqueous sodium bicarbonate and extracted three times with EtOAc. The combined organic extracts are washed with water, brine, dried (Na2SO4) and concentrated in vacuo. Purification of the crude residue by flash chromatography on silica gel affords the title compound 5e.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729104B2
Source datasetuspto-grants-2014_05
ORD IDord-23e353830e2743149b9efea4e857d1a1
Source noteuspto-grants-2014_05