HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2105029Erstellt: 25. Oktober 2026
Pentamethyldiethylenetriamine → (4-bromo-1-trityl-1H-imidazol-2-yl)(3-chloro-5-ethyl-2-fluorophenyl)methanol
https://huagongshe.com/reaction/2105029
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pentamethyldiethylenetriamine | HCID 18196 | — |
| Edukt | 2-Chloro-4-ethyl-1-fluorobenzene | HCID 18711878 | — |
| Edukt | 4-bromo-1-trityl-1H-imidazole-2-carbaldehyde | HCID 86247220 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (4-bromo-1-trityl-1H-imidazol-2-yl)(3-chloro-5-ethyl-2-fluorophenyl)methanol | HCID 68816252 | 85.857,703% |
Reaktionsschritte
To a solution of Intermediate 221.1 (100 mg, 0.631 mmol) and PMDTA (0.15 mL) in 5 mL THF at −70° C., was added BuLi (1.4 M in hexanes, 0.473 mL, 0.662 mmol). The mixture was stirred with warming to −40° C. over 30 min, recooled to −70° C., then a solution of Intermediate 175.1 (263 mg, 0.631 mmol) in 2 mL THF was added. The mixture was slowly warmed to −20° C. over 1 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 40% EtOAc/hexanes gradient) to afford 312 g of Intermediate 221.2 as a colorless solid. LCMS (50 to 100% B, 4 min gradient, A=95% H2O/5% CH3CN/0.1% TFA, B=5% H2O/95% CH3CN/0.1% TFA) RT=5.45 min, 575.28 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07576098B2 |
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| Quelldatensatz | uspto-grants-2009_08 |
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| ORD ID | ord-3cfa38135adf4a4b9a61ce3eb6ddf110 |
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| Quellennotiz | uspto-grants-2009_08 |
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