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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097773Generated: October 31, 2026

Triphenylphosphine → HCID 59277723, compound

https://huagongshe.com/reaction/1097773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 1H-imidazole-5-carboxylateHCID 565661—
ReactantHCID 3472400HCID 3472400—
Reactant4-Hydroxy-3,3-dimethyl-3,4-dihydro-1H-quinolin-2-oneHCID 59277712—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59277723HCID 59277723—

Reaction Steps

A solution of di-butyl azodicarboxylate (145 mg, 0.6275 mmol) in 2 mL of dry THF is added dropwise to a suspension of 3H-Imidazole-4-carboxylic acid methyl ester (79 mg, 0.6275 mmol), PPh3 (165 mg, 0.6275 mmol), and 4-Hydroxy-3,3-dimethyl-3,4-dihydro-1H-quinolin-2-one (80 mg, 0.418 mg) in 3 mL of dry THF at 0° C. The resulting mixture is slowly warmed up to room temperature, and stirred for 2 h. The reaction is quenched with 2 M HCl and stirred for another 0.5 h. After concentration, the residue is dissolved in HCl (2 M) and extracted with ethyl acetate (20 mL×3). The aqueous layer is adjusted to pH 8-9 by addition of saturated NaHCO3 solution. Subsequently, the mixture is extracted with ethyl acetate (20 mL×3). The combined extracts are washed with brine, and dried over anhydrous Na2SO4. After concentration, the residue is purified by flash column first then by reverse phase HPLC and gives two title regioisomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143278B2
Source datasetuspto-grants-2012_03
ORD IDord-81c8d230859d421d99759cf71235bd62
Source noteuspto-grants-2012_03