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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191577Generated: November 1, 2026

1,3-Bis(diphenylphosphino)propane → HCID 68488910, compound

https://huagongshe.com/reaction/1191577

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 49787146HCID 49787146—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 68488910HCID 68488910275.7%

Reaction Steps

A solution of 4-(4-bromo-4′-chlorobiphenyl-3-yl)-2,2,6,6-tetramethylpyran-3,5-dione (0.314 g, 0.72 mmol), vinylboronic anhydride pyridine complex (0.175 g, 0.73 mmol), lithium hydroxide monohydrate (0.177 g, 4.22 mmol), 1,3-bis(diphenylphosphino)propane (0.015 g, 0.036 mmol) and palladium acetate (0.010 g, 0.044 mmol) is stirred in a mixed solvent system of 1,2-dimethoxyethane (5 ml) and distilled water (1 ml) at 80° C. for 3 hours. After cooling to room temperature the mixture is filtered through diatomaceous earth, followed by washing with ethyl acetate and distilled water. The aqueous phase is acidified with 2M aqueous hydrochloric acid to pH3, then the organic phase is separated and the aqueous phase extracted again with ethyl acetate. All organic fractions are combined, then dried over anhydrous magnesium sulphate and filtered. After concentration in vacuo the crude oil is purified by preparative reverse phase HPLC then triturated with hexanes to afford 4-(4′-chloro-4-vinylbiphenyl-3-yl)-2,2,6,6-tetramethylpyran-3,5-dione (0.038 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680012B2
Source datasetuspto-grants-2014_03
ORD IDord-e68e1f53e0a942f891c2843ab7334185
Source noteuspto-grants-2014_03