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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642111Generated: October 26, 2026

4-Aminobenzoic Acid → HCID 18405738, compound

https://huagongshe.com/reaction/642111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantDiisopropylethylamineHCID 81531—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantTerephthalic acid monomethylester chlorideHCID 53442854—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18405738HCID 1840573864%

Reaction Steps

To a solution of 4-aminobenzoic acid (500 mg, 3.65 mmol) in anhydrous THF (20 mL) were added DIEA (1.36 mL, 8.02 mmol) and tert-butyldimethylchlorosilane (4 mL, 1M in THF). The resulting mixture was allowed to stir at rt for 45 min. A solution of terephtalic acid monomethyl ester chloride (800 mg, 4 mmol) in THF (5 mL) was added and the resulting mixture was stirred for 90 min at rt until the disappearance of the starting material and finally TBAF (4 mL, 1M in THF) was added. After 25 min at rt, the reaction was quenched with a solution of 0.1N HCl (100 mL). Extraction with EtOAc (3×200 mL), drying over sodium sulfate and evaporation under vacuo gave a pale yellow solid. Washing with hot EtOH (50 mL) gave the tilte compound as a white solid (698 mg, 64%) in a 84% purity by HPLC (MaxPlot detection between 230 and 400 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696231B2
Source datasetuspto-grants-2010_04
ORD IDord-25caaf818bf04494b7b2ba1600f1c3e3
Source noteuspto-grants-2010_04