HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052325Generated: October 26, 2026
Hydrochloric Acid → 2-(Methacryloyloxy)ethyl 2-acetylpent-2-enoate
https://huagongshe.com/reaction/1052325
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-(Acetoacetoxy)ethyl methacrylate | HCID 88855 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Methacryloyloxy)ethyl 2-acetylpent-2-enoate | HCID 123506831 | — |
Reaction Steps
To a magnetically stirred, 1000 mL, round bottom flask were added 200 mL of propionaldehyde and 587 mL 2-(methacryloyloxy)ethyl 3-oxobutanoate. The reaction mixture was cooled to 0° C., in an ice bath, and then 3 to 5 mL of piperidine was added dropwise over one minute. The mixture was stirred at 0° C., for 2 hours, and then allowed to warm to room temperature over the course of 2-2.5 hours. To the reaction mixture was slowly added 30 mL of 3N HCl, over about one minute, to neutralize the piperdine. The mixture was poured into a separatory funnel, and then 150 mL of deionized water was added. The mixture was shaken, and then the aqueous layer was separated and disposed of. The reaction mixture was washed three more times with 150 mL of deionized water, each time, and then dried over MgSO4. The reaction mixture was filtered, and then stabilized with 10 mass ppm of 4-hydroxy-TEMPO. The dried reaction mixture was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388260B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-ba80ac078bba4eb4a68df90d8be0075a |
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| Source note | uspto-grants-2016_07 |
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