Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095446Generated: October 31, 2026

Sodium borohydride → 5-(2-hydroxyethoxy)-5-(1-trityl-1H-imidazol-4-yl)-5,6,7,8-tetrahydronaphthalene-2-carbonitrile

https://huagongshe.com/reaction/1095446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantethyl [6-cyano-1-(1-trityl-1H-imidazol-4-yl)-1,2,3,4-tetrahydronaphthalen-1-yloxy]acetateHCID 86632962—
SolventEthanolHCID 702—
Product5-(2-hydroxyethoxy)-5-(1-trityl-1H-imidazol-4-yl)-5,6,7,8-tetrahydronaphthalene-2-carbonitrileHCID 66782193—

Reaction Conditions

Temperature20 °C

Reaction Steps

3.0 mmol of sodium borohydride are added in portions to a solution of 1.0 mmol of ethyl [6-cyano-1-(1-trityl-1H-imidazol-4-yl)-1,2,3,4-tetrahydronaphthalen-1-yloxy]acetate in 5 ml of ethanol at 20° C. The reaction mixture is stirred at 20° C. for 2-6 hours and then evaporated. The residue is taken up in saturated aqueous sodium bicarbonate solution and dichloromethane, and the mixture is vigorously stirred for 10 minutes. 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 identified from the residue on the basis of its Rf by flash chromatography (SiO2 60F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138179B2
Source datasetuspto-grants-2012_03
ORD IDord-acebce3118a2471b93179e486f86a6d3
Source noteuspto-grants-2012_03