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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098564Generated: October 26, 2026

Hydrochloric Acid → HCID 68771470, compound

https://huagongshe.com/reaction/2098564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-(4-Fluorophenyl)acetic acidHCID 9837—
ReactantDiisopropylethylamineHCID 81531—
Reactantmethyl (2E)-3-(4-formylphenyl)prop-2-enoateHCID 11008713—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 68771470HCID 6877147047%

Reaction Conditions

Temperature30 °C

Reaction Steps

A mixture of 4-fluorophenylacetic acid (2.5 g, 13.2 mmol) and methyl (E)-3-(4-formylphenyl)acrylate (2.03 g, 13.2 mmol) were dissolved under stirring with acetic anhydride (8 mL). To this mixture, diisopropylethylamine (DIPEA) (3.4 mL, 19.7 mmol) was added and stirred at 30° C. for 2 hours. Upon completion (as monitored by TLC using 100% ethyl acetate as eluent), the reaction mixture was poured into water and the pH adjusted to 1 using dilute HCl (1:1). The aqueous layer was extracted with ethyl acetate (2×150 mL). The combined ethyl acetate layer was washed with water till the washings were neutral and dried over anhydrous Na2SO4. The ethyl acetate layer was evaporated to dryness to obtain a sticky compound and further triturated with cold dichloromethane (DCM) to furnish a white solid. The solid obtained was filtered and dried under vacuum to afford the title compound (2 g, 47% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450525B2
Source datasetuspto-grants-2013_05
ORD IDord-c520d875a2bf412f845d78e1d3c55cc0
Source noteuspto-grants-2013_05