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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentamethyldiethylenetriamine | HCID 18196 | — |
| Reactant | 5-Ethyl-2-fluoro-biphenyl | HCID 21432918 | — |
| Reactant | 4-bromo-1-trityl-1H-imidazole-2-carbaldehyde | HCID 86247220 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Bromo-1-trityl-1H-imidazol-2-yl)-(5-ethyl-2-fluoro-biphenyl-3-yl)-methanol | HCID 68815883 | 74.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576098B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-a0779b89c9ca47c8a9d928895df38138 |
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| Source note | uspto-grants-2009_08 |
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