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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27046Generated: October 25, 2026

Benzene → 1,2-Bis(o-anisylphenylphosphino) ethane

https://huagongshe.com/reaction/27046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantTriethylamineHCID 8471—
ReactantTrichlorosilaneHCID 24811—
Reactant1,2-Bis(o-anisylphenylphosphinyl) ethaneHCID 86734501—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product1,2-Bis(o-anisylphenylphosphino) ethaneHCID 15061558—

Reaction Steps

Reduction of 1,2-bis(o-anisylphenylphosphinyl) ethane was accomplished by refluxing 16.5 g. (0.12 mole) trichlorosilane and 12.2 g. (0.12 mole) triethylamine in 188 ml. of dry benzene for one hour. Then 3.0 g. (0.012 mole) of 1,2-bis(o-anisylphenylphosphinyl) ethane in 75 ml. of dry acetonitrile was added and the mixture refluxed 1.5 hours. Quenching in 30% sodium hydroxide solution followed by separating and evaporating the organic layer gave 1.4 g. of crude crystals which were insoluble in cold methanol. Further crystallization from hot methanol gave 1,2-bis(o-anisylphenylphosphino) ethane, m.p. 102°-104° C., [α]D20 -83.4° (C=0.5 in CHCl3). The mass spectra gave a very strong parent peak at 458 and the nmr confirmed the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220590
Source datasetuspto-grants-1980_09
ORD IDord-393e2fa1622e4648889c7113444d8e50
Source noteuspto-grants-1980_09