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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | (1-Trityl-1H-imidazol-4-yl)acetic acid | HCID 11090087 | — |
| Solvent | Ethanolamine | HCID 700 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(1-Trityl-1H-imidazol-4-yl)ethanol | HCID 10689490 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835646B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-86cf036c295542a8a466a2f4d75a1507 |
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| Source note | uspto-grants-2014_09 |
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