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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361561Generated: October 30, 2026

Hydrochloric Acid → HCID 178482907, compound

https://huagongshe.com/reaction/2361561

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 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 numberUS08691718B2
Source datasetuspto-grants-2014_04
ORD IDord-20b0e027e93a4e4a83b4c2ccdfe97a6a
Source noteuspto-grants-2014_04