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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960138Generated: October 31, 2026

Triphenyl phosphite → HCID 67448110, compound

https://huagongshe.com/reaction/1960138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenyl phosphiteHCID 7540—
Reactant(3-Bromophenyl)acetic acidHCID 74653—
Reactant1,1'-Biphenyl-4-yl-boronic acidHCID 151253—
Reactant4-Chloro-5-iodobenzene-1,2-diamineHCID 57481467—
SolventPyridineHCID 1049—
ProductHCID 67448110HCID 67448110—

Reaction Steps

To a microwave vial containing a solution of Intermediate 11-1 (which was prepared from 5-chloro-4-iodo-1,2-phenylenediamine (Intermediate 1-6 of Example 1) and 4-biphenylboronic acid following the procedures of Step 9 in Example 1) (500 mg, 1.7 mmol) in pyridine 8 mL was added 3-bromo-phenyl acetic acid (365 mg, 1.7 mmol), followed by triphenyl phosphite (0.58 mL, 2.2 mmol). The reaction was run in a microwave reactor at 220° C. for 10 min. The solvent was partially removed in vacuo, then diluted with EtOAc (75 mL) and washed three times with 50 mL portions of saturated aqueous ammonium chloride. The combined organic layers were dried (MgSO4), filtered, concentrated in vacuo, and then purified by chromatography over silica (eluting with EtOAc/Hexanes=1/1) to give the title compound 14-1 as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410284B2
Source datasetuspto-grants-2013_04
ORD IDord-839953d6c0214a98ae0d30b7060073c7
Source noteuspto-grants-2013_04