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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493221Generated: October 31, 2026

Triphenylphosphine → 5-Chloro-6-(1-isopropyl-piperidin-4-yloxy)-3-methyl-benzofuran-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/493221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Isopropylpiperidin-4-olHCID 79681—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant5-Chloro-6-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 68724257—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-6-(1-isopropyl-piperidin-4-yloxy)-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 6872362494.8%

Reaction Steps

The above prepared 5-chloro-6-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester (0.700 g, 2.75 mmol) was dissolved in 12 mL of THF and treated successively at −10° C. with 1-isopropyl-piperidin-4-ol (0.551 g, 1.4 eq.), triphenylphosphine (1.001 g, 1.4 eq.) and DIAD (0.755 mL, 1.4 eq.), and the mixture then kept at ambient temperature for another 4 h. Pouring onto crashed ice/NH4Cl, twofold extraction with AcOEt, washing with water and brine, drying over magnesium sulfate, and evaporation of the solvents, followed by flash chromatography (SiO2, NEt3/AcOEt=2/98), produced 0.990 g of the title compound as light yellow gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534788B2
Source datasetuspto-grants-2009_05
ORD IDord-0d504c4eecf64e069f6c3c3da0c24b7f
Source noteuspto-grants-2009_05