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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54971Generated: October 28, 2026

Water → 2-(2-Thienylcarbonyl)benzoic acid

https://huagongshe.com/reaction/54971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhthalic AnhydrideHCID 6811—
ReactantThiopheneHCID 8030—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventNitrobenzeneHCID 7416—
Product2-(2-Thienylcarbonyl)benzoic acidHCID 28265427%

Reaction Steps

A solution of 74.1 g (0.5 mole) of phthalic anhydride in 300 mL of nitrobenzene was treated with 147 g (1.1 mole) of aluminum chloride. The solution was stirred for two hours and 42.1 g (0.5 mole) of thiophene was added dropwise over 80 minutes at 40°-45°. The reaction was stirred at 50°-55° for two hours and then let sit at room temperature overnight. The reaction was poured into 2.8 L of cold water, stirred, separated, and the nitrobenzene was removed from the nitrobenzene layer by steam distillation. The residue was recrystallized from toluene to provide 31.1 g (27%) of 2-thienoylbenzoic acid, mp 141-143. The thienoylbenzoic acid was treated with methylhydrazine as described in Example 185 to provide 24.4 g (75%) of the phthalazinone product, mp 143-144, after recrystallization from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624922
Source datasetuspto-grants-1997_04
ORD IDord-badfe0d6a3f14dbbb8f39bceae2caad5
Source noteuspto-grants-1997_04