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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480467Generated: October 29, 2026

Tetrahydrofuran → 1-(1H-Imidazol-4-yl)-1-(naphtho[2,1-b]furan-7-yl)-2-methyl-1-propanol

https://huagongshe.com/reaction/480467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
ReactantMagnesiumHCID 5462224—
Reactant7-Bromonaphtho[2,1-b]furanHCID 18769051—
Product1-(1H-Imidazol-4-yl)-1-(naphtho[2,1-b]furan-7-yl)-2-methyl-1-propanolHCID 178450055—

Reaction Conditions

Temperature0 °C

Reaction Steps

Iodomethyl (0.05 mL) was added to mixture THF (5 mL) and magnesium (turnings, 0.719 g) with stirring. 7-bromonaphtho[2,1-b]furan (6.09 g) was added and the mixture was refluxed for 2 h. The resulting mixture was cooled to 0° C. and a solution of 4-formyl-1-trityl-1H-imidazole (4.71 g) in THF (40 mL) was added. The mixture was stirred at room temperature for 1 h and aq. ammonium chloride was added. The mixture was extracted with ethyl acetate, dried and concentrated. The residue was chromatographed on silica gel (eluent; hexane:ethyl acetate=2:1→1:2) to give the titled compound (2.30 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649643B1
Source datasetuspto-grants-2003_11
ORD IDord-d04ce16a99e44ef1b3727f730ae8150f
Source noteuspto-grants-2003_11