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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247738Generated: November 2, 2026

4-Phenoxybenzoic acid → HCID 68521959, compound

https://huagongshe.com/reaction/2247738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenoxybenzoic acidHCID 75182—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86620224HCID 86620224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68521959HCID 68521959—

Reaction Steps

The crude product of the title compound was synthesized by conducting the similar reaction to that mentioned in Example 5 (5a) using 4-phenoxybenzoic acid (0.16 g, 0.73 mmol), 1-hydroxybenzotriazole (0.12 g, 0.76 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.15 g, 0.76 mmol), 4-ethyl-N′-hydroxy-5-[(tetrahydro-2H-pyran-2-yloxy)methyl]thiophene-2-carboximidamide (0.17 g, 0.69 mmol) that was obtained in Example 22 (22d) and tetrabutylammonium fluoride (a 1.0 M solution in tetrahydrofuran, 14 ml, 1.4 mmol). Subsequently, the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (0:10 to 2:8) as the eluent to afford the title compound (0.25 g) in a yield of 78% as a colourless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687491B2
Source datasetuspto-grants-2010_03
ORD IDord-2ce976adf07b40d1879e56f89a27df2b
Source noteuspto-grants-2010_03