Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875291Generated: October 29, 2026

Hydrochloric Acid → HCID 178482907, compound

https://huagongshe.com/reaction/875291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant4-bromo-N,N-dimethylanilineHCID 11465—
ReactantDiethylphosphiteHCID 3780918—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178482907HCID 17848290752.9%

Reaction Conditions

Temperature5 °C

Reaction Steps

Under an argon atmosphere, a solution of magnesium (3.0 g, 1.0 equivalent) and a small amount of iodine in 75 tetrahydrofuran (30 mL) was stirred at room temperature for 1 hr. After addition of 4-bromo-N,N-dimethylaniline (25 g, 0.125 moL) at 45° C., the mixture was stirred at 5° C. for 1 hr. After addition of diethyl phosphite (8.63 g, 0.50 equivalent) at 5° C., the mixture was stirred at 5° C. for 1 hr. Water (30 mL) was added to the mixture at 3° C., and toluene (60 mL) and 6M hydrochloric acid (30 mL) were added thereto, and the mixture was stirred at room temperature for 30 min. The reaction mixture was partitioned, and the aqueous layer was neutralized with sodium hydroxide and extracted with tetrahydrofuran (30 mL). Then, the combined organic layer was dried over anhydrous magnesium sulfate and filtered naturally, and the filtrate was concentrated under reduced pressure. The residue was recrystallized from diisopropyl ether to give the title compound (9.53 g, slightly brown white crystals). yield 52.9%. melting point 152.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981147B2
Source datasetuspto-grants-2015_03
ORD IDord-a51c230bc18d46a58c671240b80b4724
Source noteuspto-grants-2015_03