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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937801Generated: October 30, 2026

Chlorodicyclohexylphosphine → 2-(Dicyclohexylphosphino)-2'-methoxybiphenyl

https://huagongshe.com/reaction/1937801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodicyclohexylphosphineHCID 2734135—
Reactant2-bromo-2'-methoxy-1,1'-BiphenylHCID 12040724—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(Dicyclohexylphosphino)-2'-methoxybiphenylHCID 1179418654.4%

Reaction Steps

A solution of 2-bromo-2′methoxy-1,1′-biphenyl (535 mg, 2.03 mmol) in THF (20 mL) was cooled to −78° C. under argon, then n-BuLi (1.6 M in hexane, 1.35 mL, 2.16 mmol) was added dropwise. After 2.5 h at −78° C., a solution of chlorodicyclohexylphosphine (570 mg, 2.45 mmol) in THF (3 mL) was added over 10 min. The reaction mixture was then allowed to warm to room temperature overnight, then quenched with saturated aqueous NaHCO3 and concentrated in vacuo. The resulting aqueous suspension was extracted with ether (2×50 mL), and the combined ethereal layers were dried (Na2SO4), filtered and concentrated in vacuo. The resulting crude solid was recrystallized from ethanol to afford 420 mg (54 %) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395916B1
Source datasetuspto-grants-2002_05
ORD IDord-471fb367a5b14adbbb66348d72fa5d4b
Source noteuspto-grants-2002_05