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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dimethoxybenzene | HCID 9025 | — |
| Reactant | 1-Bromo-2-chlorobenzene | HCID 12754 | — |
| Reactant | Chlorodicyclohexylphosphine | HCID 2734135 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563548B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-f91a150793bc4f2fafdf752a48cbf6af |
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| Source note | uspto-grants-2013_10 |
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