HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420238Generated: October 26, 2026
Hydrochloric Acid → Ethyl 2-(1-hydroxycyclohex-2-en-1-yl)acetate
https://huagongshe.com/reaction/420238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Cyclohexen-1-one | HCID 13594 | — |
| Reactant | HCID 178472539 | HCID 178472539 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(1-hydroxycyclohex-2-en-1-yl)acetate | HCID 566443 | 87% |
Reaction Steps
Under nitrogen atmosphere, 20 mL of ethyl acetate was added to 3.05 g (5 mmol, 1.0 equivalent) of (BrZnCH2COOEt.THF)2. Under argon atmosphere, a solution of 0.48 g (5 mmol) of 2-cyclohexen-1-one in 5 mL of ethyl acetate was added dropwise while stirring at 0˜5° C. The mixture was stirred at 0˜5° C. for 3 hours. 10 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 (×2) of an aqueous saturated sodium chloride solution, 10 mL (×2) of an aqueous saturated sodium bicarbonate solution, and 10 mL of an aqueous saturated sodium chloride solution. After washing, the organic layer was dried with anhydrous magnesium sulfate. Concentration under reduced pressure afforded 0.80 g of the desired product (yield 87%).
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-f231fe79055847a1b26a3b7c452af06a |
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| Source note | uspto-grants-2012_01 |
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