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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105033Generated: October 26, 2026

Pentamethyldiethylenetriamine → (4-Bromo-1-trityl-1H-imidazol-2-yl)-(5-ethyl-2-fluoro-biphenyl-3-yl)-methanol

https://huagongshe.com/reaction/2105033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentamethyldiethylenetriamineHCID 18196—
Reactant5-Ethyl-2-fluoro-biphenylHCID 21432918—
Reactant4-bromo-1-trityl-1H-imidazole-2-carbaldehydeHCID 86247220—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-1-trityl-1H-imidazol-2-yl)-(5-ethyl-2-fluoro-biphenyl-3-yl)-methanolHCID 6881588374.1%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of Intermediate 228.2 (85 mg, 0.424 mmol) and PMDTA (0.10 mL, 0.478 mmol) in 4 ml THF at −78° C., was added BuLi (1.4 M in hexanes, 0.334 mL, 0.467 mmol). The mixture was stirred with warming to −40° C. over 30 min, recooled to −78° C., then a solution of Intermediate 175.1 (177 mg, 0.424 mmol) in 1.5 mL THF was added. The mixture was warmed to rt over 0.5 h. The reaction was quenched with sat. NH4Cl, then was diluted with EtOAc. The organic phase was washed with H2O (2×) and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 30% EtOAc/hexanes gradient) to afford 194 mg of Intermediate 228.3 as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576098B2
Source datasetuspto-grants-2009_08
ORD IDord-a0779b89c9ca47c8a9d928895df38138
Source noteuspto-grants-2009_08