HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243866Generated: November 2, 2026
Allyl bromide → Methyl 3-(4-(allyloxy)phenyl)-3-(ethoxyimino)propanoate
https://huagongshe.com/reaction/2243866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-(ethoxyimino)-3-(4-hydroxyphenyl)propanoate | HCID 136360155 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-(4-(allyloxy)phenyl)-3-(ethoxyimino)propanoate | HCID 72531910 | — |
Reaction Steps
To a solution of crude methyl 3-(ethoxyimino)-3-(4-hydroxyphenyl)propanoate obtained from Step A at 0° C. was added allyl bromide (0.65 mL) and potassium carbonate (781 mg) in DMF (5 mL), and the resulting suspension was stirred at 0° C. for 2 h. Ethyl acetate and water were added, the aqueous layer was extracted with ethyl acetate (×3), and the combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered, and evaporated in vacuo to give the title compound as an oil. The crude product was used in Step C without purification. HPLC retention time: 1.88 min (method A). MS (ESI) (M+H)+ 278.14.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678784B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-12e2caa0a57e4a988e30117271ef2af7 |
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| Source note | uspto-grants-2010_03 |
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