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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361384Generated: October 30, 2026

Hexachloroethane → HCID 57549753, compound

https://huagongshe.com/reaction/1361384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 59596729HCID 59596729—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57549753HCID 5754975386.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium (2.5M in hexanes, 3.3 mL) was added to a solution of 4,5-dibromo-2-ethoxy-1-(2-trimethylsilanylethoxymethyl)-1H-imidazole (3.0 g, 7.5 mmol) and N,N,N′,N′-tetramethylethylenediamine (1.2 mL, 8.3 mmol) in THF (20 mL) at −78° C. After 3 minutes, a solution of hexachloroethane (2.3 g, 9.7 mmol) in THF (8 mL) was added at −78° C. The mixture was stirred at −78° C. for 1 hour and was then allowed to warm to room temperature. Saturated aq. NH4Cl (3 mL) was added and the mixture was concentrated in vacuo. The mixture was extracted with EtOAc (2×100 mL) and sat. aq. NaHCO3 (30 mL). The combined organic fractions were dried over Na2SO4, filtered, and concentrated in vacuo. Silica gel chromatography (EtOAc:hexane) afforded intermediate (26a) (2.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879896B2
Source datasetuspto-grants-2011_02
ORD IDord-e926928118e345a08ebb31dba8d194de
Source noteuspto-grants-2011_02