Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556182Generated: October 30, 2026

Hydrochloric Acid → HCID 178425926, compound

https://huagongshe.com/reaction/556182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant1,2-DibromoethaneHCID 7839—
Reactant3-BromotolueneHCID 11560—
ReactantDiethylphosphiteHCID 3780918—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178425926HCID 17842592693.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

Under a nitrogen stream, a solution of magnesium (3.60 g, 3.50 equivalents) and a small amount of iodine and 1,2-dibromoethane in THF (25 mL) solution was stirred at room temperature for 30 min. A solution of m-bromotoluene (25.36 g, 3.51 equivalents) in THF (130 mL) was added at 24° C., and the mixture was stirred at 40° C. for 30 min. Then, a solution of diethyl phosphite (5.84 g, 42.3 mmol) in THF (10 mL) was added at 25° C., and the mixture was stirred at 24° C. for 1.5 hrs. 6M-HCl (20 mL) was added at 4° C., and then water (20 mL) and toluene (60 mL) were added. The mixture was stirred at room temperature for 30 min. The reaction mixture was partitioned, and the organic layer was washed successively with 10% aqueous NaHCO3 solution (20 mL), water (20 mL) and 10% aqueous NaCl solution (20 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered by gravity, and further passed through a membrane filter (0.2 μm) under reduced pressure. The filtrate was concentrated under reduced pressure to give the title compound (9.09 g, colorless oil). yield 93.3%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053604B2
Source datasetuspto-grants-2011_11
ORD IDord-b77d01617b0e409fa88c1d5d7d05c013
Source noteuspto-grants-2011_11