Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254449Generated: October 26, 2026

Ethyl phenylacetate → HCID 59468695, compound

https://huagongshe.com/reaction/254449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl phenylacetateHCID 7590—
ReactantEthyl AcrylateHCID 8821—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-bromo-2-(4-methoxyphenyl)acetateHCID 10753737—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventMethyl AcrylateHCID 7294—
ProductHCID 59468695HCID 59468695—

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875643B2
Source datasetuspto-grants-2011_01
ORD IDord-c6069618c82e41d889e737ceb45ff480
Source noteuspto-grants-2011_01