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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476326Generated: October 25, 2026

1,2-Bis(dichlorophosphino)benzene → 1,2-Bis(bis(3,5-bis(2,6-dimethylphenyl)phenyl)phosphino)benzene

https://huagongshe.com/reaction/476326

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Bis(dichlorophosphino)benzeneHCID 3316562—
ReactantMagnesiumHCID 5462224—
Reactant2~5~-Bromo-1~2~,1~6~,3~2~,3~6~-tetramethyl-1~1~,2~1~:2~3~,3~1~-terphenylHCID 15471339—
SolventTetrahydrofuranHCID 8028—
Product1,2-Bis(bis(3,5-bis(2,6-dimethylphenyl)phenyl)phosphino)benzeneHCID 86654813—

Reaction Steps

1-Bromo-3,5-bis(2,6-dimethylphenyl)benzene (2.74 g, 7.50 mmol) was added dropwise to magnesium (0.28 g, 11.52 mmol) and THF (10 mL) in an argon atmosphere. After the dropwise addition, the mixture was heated under reflux for 1 hour. The reaction mixture was cooled to ambient temperature and filtered, and the thus-obtained THF solution of 1-(3,5-bis(2,6-dimethylphenyl))magnesium bromide, and 1,2-bis(dichlorophosphino)benzene (0.28 g, 1.00 mmol) were reacted as in Production Example 1. The reaction was allowed to proceed overnight at 60° C. After purification, the title compound was obtained as a yellow powder (0.70 g, yield 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637710B2
Source datasetuspto-grants-2014_01
ORD IDord-0001196f94c947389f8fd96cac58b106
Source noteuspto-grants-2014_01