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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270217Generated: October 30, 2026

Phthalic Anhydride → HCID 68860548, compound

https://huagongshe.com/reaction/270217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantHCID 68836937HCID 68836937—
SolventAcetic AcidHCID 176—
ProductHCID 68860548HCID 68860548—

Reaction Steps

A mixture of 2-amino-4-[2-(4-bromophenyl)ethyl]-5-methyl-thiophene-3-carboxylic acid ethyl ester (2 mmol, Example 30, Part B) and phthalic anhydride (2.2 mmol) in glacial acetic acid (20 mL) is heated at reflux overnight. After cooling to room temperature, the acetic acid is removed in vacuo and the residue triturated with petroleum ether. The crude product is collected by filtration, suspended in acetyl chloride (5 mL), and heated to reflux for one hour. After removing the solvent in vacuo, the residue is dissolved in ethyl acetate (30 mL), washed sequentially with 5% aqueous NaHCO3 (10 mL), water (10 mL), brine (10 mL), dried (Na2SO4), filtered, and concentrated in vacuo. Recrystallization affords the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449490B2
Source datasetuspto-grants-2008_11
ORD IDord-a14f74d04adb45b7b2568565b3af94ec
Source noteuspto-grants-2008_11