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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229261Generated: October 29, 2026

3-(1-Tritylimidazol-4-YL) propionaldehyde → 1-(5-fluorobenzo[b]thiophen-2-yl)-3-(1-triphenylmethyl-1H-imidazol-4-yl)-propan-1-ol

https://huagongshe.com/reaction/2229261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-Tritylimidazol-4-YL) propionaldehydeHCID 11451428—
Reactant5-Fluoro-1-benzothiopheneHCID 11815950—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
Product1-(5-fluorobenzo[b]thiophen-2-yl)-3-(1-triphenylmethyl-1H-imidazol-4-yl)-propan-1-olHCID 1846697962.2%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of 5-fluorobenzo[b]thiophene (1.22 g) in THF (22 ml) was added n-BuLi (1.6 M solution in hexane, 5.0 ml) at −78° C., and the mixture was stirred for 1 hour. To this mixture was added a solution of 3-(1-triphenylmethyl-1H-imidazole-4-yl)propanal (2.93 g) in THF (10 ml), and the mixture was allowed to warm to −40° C. over 1 hour. The mixture was diluted with 10% aqueous ammonium chloride, warmed to room temperature, and extracted with ethyl acetate. The extract was washed with brine, dried over MgSO4, and concentrated. The residue was chromatographed on silica gel using hexane-ethyl acetate (1:1) as an eluent to give the titled compound as colorless crystals (2.58 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420375B1
Source datasetuspto-grants-2002_07
ORD IDord-643722bb0a9f41fdb56f44091c46bd8b
Source noteuspto-grants-2002_07