HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756953Generated: October 24, 2026
1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 54381600, compound
https://huagongshe.com/en/reaction/1756953
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde | HCID 618233 | — |
| Reactant | Triphenylundecylphosphonium bromide | HCID 3085198 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54381600 | HCID 54381600 | 64% |
Reaction Steps
A solution of n-BuLi (4.1 mL, 6.5 mmol, 1.6M in hexanes) was added dropwise to a suspension of n-undecyl-triphenylphosphoniumbromide (3.09 g, 6.2 mmol, obtained from triphenylphosphine and undecylbromide) in 100 mL THF at -78° C. under an atmosphere of N2. The resulting orange solution was stirred for 45 minutes before a solution of 1-(triphenylmethyl)-4-imidazolecarboxaldehyde (2.0 g, 5.9 mmol, Ref: Kelly JL, Miller CA, and McLean EW, J. Med. Chem. 1977;20:721) in 75 mL THF was added dropwise. Warmed to room temperature and stirred for 16 hours. Quenched by adding 50 mL saturated NH4Cl solution and concentrating in vacuo. The residue was partitioned between water and dichloromethane. The organic layer was dried over MgSO4, filtered, and concentrated to give a yellow oil. Chromatography (10% EtOAc/hexanes on silica) gave the title compound (1.8 g, 64% ) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05441975 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-b05c7116fe4842f4b46bea5f2dd6778f |
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| Source note | uspto-grants-1995_08 |
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