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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043554Generated: November 4, 2026

1,3-Dimethoxybenzene → 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl

https://huagongshe.com/reaction/1043554

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DimethoxybenzeneHCID 9025—
Reactant1-Bromo-2-chlorobenzeneHCID 12754—
ReactantChlorodicyclohexylphosphineHCID 2734135—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 1126987236%

Reaction Steps

To a solution of 1,3-dimethoxybenzene (2 ml, 15.30 mmol) in anhydrous THF (35 ml) at 0° C., nBuLi (6.2 ml, 15.50 mmol) is added to the dropping funnel for 5 min. The reaction medium is stirred at room temperature for 3.5 h, then 2-bromochlorobenzene (1.6 ml, 13.70 mmol) is added by syringe, dropwise, at 0° C., for 30 min. After 15 min of stirring, the reaction medium is cooled to −78° C. and nBuLi (6.20 ml, 15.50 mmol) is added to the dropping funnel dropwise for 5 min. After 30 min, chlorodicyclohexylphosphine (3.03 ml, 13.70 mmol) is added. The reaction medium is maintained at −78° C. for 1 h, under rapid stirring (mechanical stirring). After returning to room temperature, the precipitate obtained is filtered on a fritted disc containing silica topped with a layer of cellulose acetate, with 600 ml ethyl acetate. The solvents are evaporated with a rotary evaporator, and the orange oil obtained is recrystallized in acetone to obtain S-Phos ligand in the form of white crystals with a yield of 36% (1.22 g, 2.97 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563548B2
Source datasetuspto-grants-2013_10
ORD IDord-f91a150793bc4f2fafdf752a48cbf6af
Source noteuspto-grants-2013_10