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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927980Generated: November 1, 2026

Tributyltin Chloride → HCID 57468836, compound

https://huagongshe.com/reaction/1927980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 57468793HCID 57468793—
ReactantHCID 178461733HCID 178461733—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57468836HCID 5746883658%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-(4-fluoro-phenyl)-2-(4-iodo-imidazol-1-yl)-6-trifluoromethyl-pyrimidine (Example E.79) (0.87 g, 2.0 mmol) in THF (14 ml) was added at 0° C. isopropyl-magnesium chloride lithium chloride (1M in THF, 2.44 ml, 2.44 mmol). The reaction mixture was allowed to stir for 15 min at 0° C., tributyltin chloride (0.87 g, 2.67 mmol) was added, the reaction mixture was stirred at room temperature for 16 h, poured into saturated ammonium chloride solution (30 ml) and extracted with ethyl acetate (2×50 ml). The combined organic layers were washed with brine (30 ml), dried (MgSO4) and evaporated. The crude product was further purified by flash chromatography on silica gel (ethylacetate/heptane) to yield the title compound (0.69 g, 58%) as a light yellow oil. MS (ISP) 598.7 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183262B2
Source datasetuspto-grants-2012_05
ORD IDord-b410c3f4314c44cbb5b9049c755ad527
Source noteuspto-grants-2012_05