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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706650Generated: October 31, 2026

Ethyl (3-Hydroxyphenyl)acetate → Ethyl 3[(2-nitro-3-phenylbenzofuran-5-yl)methoxy]phenylacetate

https://huagongshe.com/reaction/1706650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (3-Hydroxyphenyl)acetateHCID 572437—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 13531604HCID 13531604—
SolventEthanolHCID 702—
ProductEthyl 3[(2-nitro-3-phenylbenzofuran-5-yl)methoxy]phenylacetateHCID 20333822—

Reaction Steps

To a solution of 0.0066 ml. of sodium ethoxide in 50 ml. of ethanol is added 1.2 g. (0.0066 mole) of ethyl 3-hydroxyphenylacetate. The mixture is heated at its reflux temperature for three hours, then 2 g. (0.006 mole) of 5-bromomethyl-2-nitro-3-phenylbenzofuran is added. The mixture is heated at its reflux temperature for 16 hours. On cooling of the reaction mixture a yellow precipitate is obtained which is separated by filtration. Recrystallization from a mixture of hexane and benzene provides ethyl 3[(2-nitro-3-phenylbenzofuran-5-yl)methoxy]phenylacetate, m.p. 67°-68° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208335
Source datasetuspto-grants-1980_06
ORD IDord-96d623536871435588460ded9c9c174c
Source noteuspto-grants-1980_06