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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706651Generated: November 3, 2026

Hydroxyphenylacetic acid → HCID 20333831, compound

https://huagongshe.com/reaction/1706651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyphenylacetic acidHCID 127—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13531604HCID 13531604—
SolventEthanolHCID 702—
ProductHCID 20333831HCID 20333831—

Reaction Steps

To a mixture of 1 g. (0.0066 mole) of 4-hydroxyphenylacetic acid and 0.53 g. of sodium hydroxide in 100 ml. of ethanol is added 2 g. (0.006 mole) of 5-bromomethyl-2-nitro-3-phenylbenzofuran, and the mixture is heated at its reflux temperature for 16 hours. The reaction mixture is evaporated to provide a residue which is extracted thoroughly with chloroform. The residue is separated from chloroform and dissolved in water. The water is acidified to pH 3. The precipitate is separated by filtration, dissolved in dichloromethane, and the dichloromethane solution is dried. The dichloromethane solution is evaporated to provide a yellow solid which is recrystallized from ethanol to provide 4-[(2-nitro-3-phenylbenzofuran-5-yl)methoxy]phenylacetic acid, m.p. 179°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208335
Source datasetuspto-grants-1980_06
ORD IDord-4ae6fc2b80e14bc39738e6ce3986ff6e
Source noteuspto-grants-1980_06