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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76862Generated: October 30, 2026

Borane;tetrahydrofuran → 2-(1-Trityl-1H-imidazol-4-yl)ethanol

https://huagongshe.com/reaction/76862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant(1-Trityl-1H-imidazol-4-yl)acetic acidHCID 11090087—
SolventEthanolamineHCID 700—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(1-Trityl-1H-imidazol-4-yl)ethanolHCID 10689490—

Reaction Conditions

Temperature0 °C

Reaction Steps

(1-Trityl-1H-imidazol-4-yl)acetic acid (65 g, 0.17 mol) is suspended in THF (400 mL) and cooled to 0° C. To this is added BH3.THF solution (350 mL, 1.0 M). The clear solution obtained is stirred at 0° C. for 30 min before warming to room temperature until LCMS indicated completion of the reaction. The solution is cooled again to 0° C. and quenched carefully with water (250 mL). The resulting solution is diluted with EtOAc (300 mL) and transferred to a separatory funnel and the aqueous layer is extracted with EtOAc. The organic phase is dried over anhydrous Na2SO4 and evaporated to give a sticky residue which is taken up in ethanolamine (800 mL) and heated to 90° C. for 2 h. The reaction is transferred to a separatory funnel, diluted with EtOAc (1 L) and washed with water (3×600 mL). The organic phase is dried over anhydrous Na2SO4 and evaporated to give 2-(1-trityl-1H-imidazol-4-yl)-ethanol as a white solid that is used as is without further purification. MS (ESI) m/z 354.8 (M+H) (prepared by alternate method in J. Med. Chem. 1996, 39(19), 3806)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835646B2
Source datasetuspto-grants-2014_09
ORD IDord-86cf036c295542a8a466a2f4d75a1507
Source noteuspto-grants-2014_09