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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349563Generated: October 30, 2026

Acetic Anhydride → 3-(4-Formyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)propionic acid

https://huagongshe.com/reaction/349563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-(4,5,6,7-Tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)propionic acidHCID 135732761—
SolventFormic AcidHCID 284—
Product3-(4-Formyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)propionic acidHCID 17962021—

Reaction Conditions

Temperature40 °C

Reaction Steps

To formic acid (50 ml) was added acetic anhydride (60 ml), and the mixture was stirred at 40° C. for 2 hours. The resulting mixture was added to the above oily product [3-(4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)propionic acid] and the mixture was stirred at room temperature for 15 hours. After evaporation of the solvent in vacuo, to the residue was added water. The mixture was neutralized with saturated aqueous sodium hydrogencarbonate solution, and concentrated in vacuo. The residue was dissolved in methanol, and the insoluble materials were removed by filtration. The filtrate was concentrated in vacuo to give 3-(4-formyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl)propionic acid (23 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179801B2
Source datasetuspto-grants-2007_02
ORD IDord-d42debacb9be480f82589e1c0222f641
Source noteuspto-grants-2007_02