HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105025Generated: October 31, 2026
Lithium diisopropylamide → (4-(2-bromophenyl)-1-trityl-1H-imidazol-2-yl)(3-(tert-butyldimethylsilyloxy)-5-ethyl-2-fluorophenyl)methanol
https://huagongshe.com/reaction/2105025
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 4-(2-bromophenyl)-1-trityl-1H-imidazole | HCID 22185143 | — |
| Reactant | 3-{[tert-Butyl(dimethyl)silyl]oxy}-5-ethyl-2-fluorobenzaldehyde | HCID 59838072 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-(2-bromophenyl)-1-trityl-1H-imidazol-2-yl)(3-(tert-butyldimethylsilyloxy)-5-ethyl-2-fluorophenyl)methanol | HCID 68815662 | 54.1% |
Reaction Steps
To a solution of Intermediate 217.1 (650 mg, 1.40 mmol) in 10 mL THF at 0° C., was added a solution of lithium diisopropylamide (2M in heptane/THF/ethylbenzene, 0838 mL, 1.68 mmol). The mixture was stirred at 0° C. for 30 min, then a solution of Intermediate 188.3 (356 mg, 1.26 mmol) in 2 mL THF. The mixture was stirred at 0° C. for 2 h, then was quenched with sat. NH4Cl and diluted with EtOAc. The organic phase was washed with H2O and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 40% EtOAc/hexanes gradient) to afford 510 mg of Intermediate 217.2 as a pale yellow 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=5.61 min, 747.67 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07576098B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-acad0d528b6945de8eb0136a07900e16 |
|---|
| Source note | uspto-grants-2009_08 |
|---|