HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254449Generated: October 26, 2026
Ethyl phenylacetate → HCID 59468695, compound
https://huagongshe.com/reaction/254449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl phenylacetate | HCID 7590 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-bromo-2-(4-methoxyphenyl)acetate | HCID 10753737 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Methyl Acrylate | HCID 7294 | — |
| Product | HCID 59468695 | HCID 59468695 | — |
Reaction Steps
To a stirred slurry of of NaH (4.4 g, 60% in mineral oil) in anhydrous Et2O (0.3 l) was added methanol (10.3 mL) followed by a solution of bromo ester obtained in Prep. 12, methyl bromo(4-methoxyphenyl)acetate (29 g) in methyl acrylate (19.8 mL) (for examples starting from an ethyl phenylacetate derivative ethanol and ethyl acrylate were used, respectively) and methanol (3 mL) at 0° C., over a 30 min. The mixture was stirred at 25° C. for 24 h and then unreacted NaH was decomposed with 3 mL methanol. Water was added (75 mL), the organic phase separated, dried over Na2SO4 and filtered. Volatiles were evaporated in vacuo to give 31.5 g of the title compound as an oil, which was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875643B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-c6069618c82e41d889e737ceb45ff480 |
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| Source note | uspto-grants-2011_01 |
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