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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619379Generated: November 2, 2026

Phenylacetic Acid → HCID 18355594, compound

https://huagongshe.com/reaction/619379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetic AcidHCID 999—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant(2-Hydroxy-5-methoxyphenyl)(4-hydroxyphenyl)methanoneHCID 15574183—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 18355594HCID 18355594—

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of (2-hydroxy-5-methoxyphenyl)-(4-hydroxyphenyl)-methanone (0.59 g, 2.42 mmol), acetic anhydride (1.15 ml, 12.1 mmol), triethylamine (0.44 ml, 3.16 mmol), and phenyl acetic acid (0.33 g, 2.42 mmol) was stirred at 135° C. for 18 h. The resulting orange coloured solution was poured into water (20 ml) and stirred for 3 h, and the resulting mixture of aqueous solution plus sticky solid was diluted with ethyl acetate (20 ml) to dissolve the solid, and the organic layer separated. The aqueous phase was further extracted with ethyl acetate (2×20 ml). The combined organic extracts were washed with water, then brine, dried over sodium sulfate and evaporated to give a yellow/orange gum. This gum was dissolved in a minimum of ether and petrol added to precipitate the title compound as an off white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05958967
Source datasetuspto-grants-1999_09
ORD IDord-c43eddd82f8748838b9354277ca95a7e
Source noteuspto-grants-1999_09