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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ethyl (2E)-4-oxo-4-phenyl-2-butenoate | HCID 5369605 | — |
| Reactant | HCID 178472539 | HCID 178472539 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | diethyl(2E)-4-hydroxy-4-phenylhex-2-enedioate | HCID 57465814 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586762B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-062f15e52cba4304bfb07d05eba02171 |
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| Source note | uspto-grants-2013_11 |
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