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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360135Generated: October 29, 2026

Acetic Acid → 4-[1-hydroxy-2-(1-trityl-1H-imidazol-4-ylmethoxy)ethyl]benzonitrile

https://huagongshe.com/reaction/1360135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant4-[2-(1-trityl-1H-imidazol-4-ylmethoxy)acetyl]benzonitrileHCID 66782326—
SolventEthanolHCID 702—
Product4-[1-hydroxy-2-(1-trityl-1H-imidazol-4-ylmethoxy)ethyl]benzonitrileHCID 66782189—

Reaction Steps

Sodium borohydride is added in portions to a solution of 1 mmol of 4-[2-(1-trityl-1H-imidazol-4-ylmethoxy)acetyl]benzonitrile in 12 ml of ethanol at 0° C. The reaction solution is stirred at room temperature for 12 hours, then poured into ice-water and stirred for 15 minutes. The mixture is adjusted to pH 5 by adding glacial acetic acid and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed with water and brine, dried over sodium sulphate and evaporated. The title compound is identified from the residue on the basis of the Rf by flash chromatography (SiO2 60F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879847B2
Source datasetuspto-grants-2011_02
ORD IDord-be2ee89089ec47aaa9946c0d29187221
Source noteuspto-grants-2011_02