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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471355Generated: October 31, 2026

Aspirin → 2-Acetoxybenzoyl chloride

https://huagongshe.com/reaction/1471355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAspirinHCID 2244—
ReactantThionyl ChlorideHCID 24386—
Product2-Acetoxybenzoyl chlorideHCID 79668—

Reaction Conditions

Temperature80 °C

Reaction Steps

Acetyl salicylic acid (1.0 g) was mixed with thionyl chloride (1.0 mL) and mixture was heated in a 50 mL round bottom flask under nitrogen at 80° C. for 1 hour. The excess thionyl chloride was removed by distillation, dried in high vacuum to get acetyl salicyloyl chloride as a viscous liquid, ˜1.1 g. Used for next step with out further purification. Curcumin (0.50 g) was taken in 10 mL of DMF in a 50 mL round bottom flask under nitrogen and pyridine was added. Acetyl salicyloyl chloride (˜1.1 g) was taken in 5 mL of DMF and was added drop wise from a pressure equalizing separating funnel. The solution turned darker in color. The mixture was heated at 90° C. for 1 hour and then at room temperature overnight. To the reaction mixture 100 mL of water was added. A solid formed which was filtered, the solid was stirred with 30 mL of NaHCO3 solution. The solid was filtered, washed with water, dried under high vacuum to yield 1.10 g of the product, curcumin acetyl salicylate or curcumin-aspirin, NMR was consistent with the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012411B2
Source datasetuspto-grants-2015_04
ORD IDord-9df5a65348c84b4282e49c290ee2673d
Source noteuspto-grants-2015_04