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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875280Generated: October 29, 2026

Iodine → HCID 178429638, compound

https://huagongshe.com/reaction/875280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1,2-DibromoethaneHCID 7839—
Reactant4-bromo-N,N,2,6-tetramethylanilineHCID 142731—
ReactantDiethylphosphiteHCID 3780918—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178429638HCID 17842963840%

Reaction Conditions

Temperature40 °C

Reaction Steps

Under an argon atmosphere, a solution of magnesium (2.4 g, 0.75 equivalent), a small amount of iodine and a small amount of 1,2-dibromoethane in tetrahydrofuran (15 mL) was stirred at room temperature for 1 hr. A solution of 4-bromo-N,N,2,6-tetramethylaniline (31.2 g, 0.137 moL) synthesized in Reference Example 2 in tetrahydrofuran (50 mL) was added to the mixture at 25° C. to 30° C. over 1 hr, and the mixture was stirred at 40° C. for 1 hr. Then, a solution of diethyl phosphite (4.69 g, 0.25 equivalent) in tetrahydrofuran (15 ml) was added at 25° C. to 30° C. over 1 hr. Water (60 mL) was added to the mixture at 0° C. to 5° C., and then toluene (100 mL) was added to the mixture, and the insoluble material was removed by filtration. The filtrate was partitioned, and the organic layer was washed with water (30 mL) and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel 100 g, n-hexane/ethyl acetate) to give the title compound (4.6 g, colorless liquid). yield 40%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981147B2
Source datasetuspto-grants-2015_03
ORD IDord-84f6ec3e2ef7495e9672142134298b07
Source noteuspto-grants-2015_03