Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680706Generated: November 2, 2026

Benzene → HCID 12902869, compound

https://huagongshe.com/reaction/1680706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantEthyl 2-chloroacetoacetateHCID 11858—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 4-(4-hydroxyphenyl)phenylacetateHCID 23455887—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 12902869HCID 12902869—

Reaction Steps

To a solution of 0.25 mole of sodium ethoxide is added 64 g. (0.25 mole) of ethyl 4-(4-hydroxyphenyl)phenylacetate. After stirring two hours the solution is evaporated, benzene is added, and the solution is further evaporated. The residue is dissolved in 800 ml. of benzene, 0.25 mole of ethyl α-chloroacetoacetate is added, and the mixture is stirred at room temperature, then heated at its reflux temperature for 16 hours and filtered hot. Evaporation provides a residue which is dissolved in carbon tetrachloride and filtered through silica gel. This intermediate is treated with concentrated sulfuric acid at 0° C. After stirring one hour, ice is added and the mixture is extracted with benzene. The benzene layer is dried, then evaporated. The residue is recrystallized from a dichloromethanehexane mixture, then carbon tetrachloride, to provide ethyl 4-(2-ethoxycarbonyl 3-methylbenzofuran-5-yl)phenylacetate, m.p. 110°-112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04275221
Source datasetuspto-grants-1981_06
ORD IDord-a8d94d7218d342e0b39cd7a4f7e5f820
Source noteuspto-grants-1981_06