Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712910Generated: November 1, 2026

Sodium borohydride → HCID 68440362, compound

https://huagongshe.com/reaction/1712910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86626005HCID 86626005—
SolventEthanolHCID 702—
ProductHCID 68440362HCID 68440362—

Reaction Steps

2.45 mmol of sodium borohydride are added to a solution of 1.63 mmol of ethyl [(4-cyanophenyl)-1-(trityl-1H-imidazol-4-yl)methoxy]acetate in 10 ml of ethanol at room temperature. The reaction mixture is stirred at room temperature for 16 hours and then evaporated. The residue is taken up in dichloromethane and saturated aqueous sodium bicarbonate solution, the phases are separated, and the aqueous phase is back-extracted with dichloromethane. The combined organic phases are dried with sodium sulphate and evaporated. The title compound is obtained as a white solid from the residue by flash chromatography (SiO2 60F). Rf=0.10 (ethyl acetate-heptane 1:2); Rt=7.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795253B2
Source datasetuspto-grants-2010_09
ORD IDord-ca914870585749d3903f35d179c9e520
Source noteuspto-grants-2010_09