HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420236Generated: October 31, 2026
Hydrochloric Acid → HCID 57465815, compound
https://huagongshe.com/reaction/420236
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (E)-3-Nonen-2-one | HCID 5317045 | — |
| Reactant | HCID 178472539 | HCID 178472539 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57465815 | HCID 57465815 | 99% |
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 0.70 g (5 mmol) of trans-3-nonen-2-one 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. 8.5 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 1.13 g of the desired product (yield 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093403B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-0fc1f594d4814f2590f8ea1b0a3e234e |
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| Source note | uspto-grants-2012_01 |
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