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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964489Generated: October 29, 2026

1-Bromo-2-iodobenzene → HCID 58239414, compound

https://huagongshe.com/reaction/1964489

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-iodobenzeneHCID 11415—
ReactantBIS(3,5-DIMETHYLPHENYL)CHLOROPHOSPHINEHCID 4187520—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 58239414HCID 5823941456%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 9.67 g (34.2 mmol) of 1-bromo-2-iodobenzene in 30 ml of THF are added dropwise, at −78° C., 17.6 ml (37.6 mmol) of an isopropylmagnesium chloride solution (2 molar in THF). The mixture is stirred at a temperature between −30° C. and −40° C. for a further 1 hour, then cooled again to −78° C., and a suspension of 10.4 g (37.6 mmol) of bis(3,5-dimethylphenyl)chlorophosphine in 10 ml of THF and 10 ml of TBME are added. The cooling is removed and the reaction mixture is stirred at room temperature overnight. The resulting solution is admixed with 50 ml of water and extracted with water/TBME. The organic phases are collected and dried over sodium sulphate, and the solvent is distilled off under reduced pressure on a rotary evaporator. The solid white crude product is purified by chromatography (silica gel 60; eluent=methylene chloride). The desired product is obtained as a white solid in a yield of 56%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415488B2
Source datasetuspto-grants-2013_04
ORD IDord-08f372f74d4a410e8cda77e765f46122
Source noteuspto-grants-2013_04