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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983841Generated: November 1, 2026

Hydrochloric Acid → HCID 178527026, compound

https://huagongshe.com/reaction/1983841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant1,2-DibromoethaneHCID 7839—
Reactant2-BromonaphthaleneHCID 11372—
ReactantDiethylphosphiteHCID 3780918—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178527026HCID 17852702653%

Reaction Conditions

Temperature40 °C

Reaction Steps

Under an argon atmosphere, a solution of magnesium (2.94 g, 2.00 equivalents), a slight amount of iodine and 1,2-dibromoethane in tetrahydrofuran (60 mL) was stirred at a room temperature for 1 hour. After addition of a solution of 2-bromonaphthalene (25.00 g, 2.00 equivalent) in tetrahydrofuran (20 mL) at 27° C., the mixture was stirred at 40° C. for 45 minutes. Then, after addition of a solution of diethyl phosphite (9.77 g, 0.06 mol) in tetrahydrofuran (10 mL) at −9° C., the mixture was stirred at 2° C. for 3 hours. Further, water (20 mL) was added thereto at −5° C., followed by further addition of toluene (60 mL) and 6M-HCl (20 mL). The resulting mixture was separated into layers, and the organic layer obtained was successively washed with an aqueous 5% NaHCO3 solution and an aqueous 5% NaCl solution. The organic layer was dried over dehydrated magnesium sulfate and then spontaneously filtered, and the filtrate obtained was concentrated under reduced pressure. The residue was recrystallized from isopropyl ether/n-hexane and dried (under reduced pressure at 40° C.) to obtain the titled compound (9.621 g, white powder). The yield was 53.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541498B2
Source datasetuspto-grants-2009_06
ORD IDord-5628e6afea2d47b58a42dcf74717235c
Source noteuspto-grants-2009_06