Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556176Generated: October 30, 2026

Hydrochloric Acid → HCID 178527031, compound

https://huagongshe.com/reaction/556176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantDiethylphosphiteHCID 3780918—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178527031HCID 17852703135.3%

Reaction Conditions

Temperature3 °C

Reaction Steps

Under an argon atmosphere, a solution of magnesium (6.95 g, 1.0 equivalent) and a small amount of iodine in THF (70 mL) was stirred at room temperature for 1 hr. 1-Bromo-4-fluorobenzene (50 g, 0.286 moL) was added at 40° C., and the mixture was stirred at 3° C. for 1 hr. Then, diethyl phosphite (19.7 g, 0.50 equivalents) was added at 13 to 19° C., and the mixture was stirred at 5° C. for 1 hr. Water (45 mL) was added at 4° C., and toluene (150 mL) and 6M-HCl (45 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 water, 5% aqueous NaHCO3 solution (50 mL), and 5% aqueous NaCl solution (50 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered by gravity, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica gel 30 g, n-hexane/ethyl acetate=1/0→3/1) to give the title compound (12.0 g, pale-red oil). yield 35.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053604B2
Source datasetuspto-grants-2011_11
ORD IDord-c99772246b79445d91c5ce9174d8e42e
Source noteuspto-grants-2011_11