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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044787Generated: October 25, 2026

Hydrochloric Acid → diethyl(2E)-4-hydroxy-4-phenylhex-2-enedioate

https://huagongshe.com/reaction/2044787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl (2E)-4-oxo-4-phenyl-2-butenoateHCID 5369605—
ReactantHCID 178472539HCID 178472539—
SolventTetrahydrofuranHCID 8028—
Productdiethyl(2E)-4-hydroxy-4-phenylhex-2-enedioateHCID 5746581497%

Reaction Steps

Under nitrogen atmosphere, 15 mL of THF was added to 3.05 g (5 mmol, 1.0 equivalent) of (BrZnCH2COOEt.THF)2. Under argon atmosphere, a solution of 1.02 g (5 mmol) of trans-ethyl 3-benzoylacrylate in 2.5 mL of THF was added dropwise while stirring at 0˜5° C. The mixture was stirred at 20˜25° C. for 3 hours. 7.5 mL of 1N hydrochloric acid was added dropwise at 20° C. or lower, followed by dilution with 25 mL of ethyl acetate. Then, the layers were separated. The organic layer was washed successively with 5 mL (×2) of 1N hydrochloric acid, 5 mL of water, 10 mL (×2) of an aqueous saturated sodium bicarbonate solution, and 5 mL (×2) of an aqueous saturated sodium chloride solution. After washing, the organic layer was dried with anhydrous magnesium sulfate. Concentration under reduced pressure afforded 1.42 g of the desired product (yield 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586762B2
Source datasetuspto-grants-2013_11
ORD IDord-062f15e52cba4304bfb07d05eba02171
Source noteuspto-grants-2013_11