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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199544Generated: October 31, 2026

Iodine → HCID 19867068, compound

https://huagongshe.com/reaction/1199544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 14450301HCID 14450301—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 19867068HCID 19867068—

Reaction Steps

n-Butyllithium (2.94 cm3 of a 1.43M solution in n-hexane) was added dropwise to a stirred suspension of 6-(4-methylimidazol-1-yl)-8-methyl-2-(1H)-quinolone (0.45 g) (see Example 6) in tetrahydrofuran (THF) (25 cm3) at -70° C. under nitrogen. After one hour iodine (0.51 g) was added and the mixture warmed to room temperature over 1.5 hours. Ammonium chloride solution was added (5 cm3), and the mixture was poured into water (20 cm3). The aqueous mixture was extracted with dichloromethane (3×50 cm3) and the combined and dried (MgSO4) organic extracts were evaporated in vacuo to give a residue which was chromatographed on silica (Merck "MK 60.9385" [Trade Mark]). Elution with chloroform followed by combination and evaporation of appropriate fractions gave a solid which was recrystallised from ethyl acetate to afford 6-(2-iodo-4-methylimidazol-1-yl)-8-methyl-2-(1H)-quinolone, m.p. (d) 260° (0.22 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04900839
Source datasetuspto-grants-1990_02
ORD IDord-7252f589aba845be808e39d08112a65c
Source noteuspto-grants-1990_02