Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637807Generated: November 1, 2026

Phenylacetic Acid → HCID 18355594, compound

https://huagongshe.com/reaction/1637807

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 numberUS06043269
Source datasetuspto-grants-2000_03
ORD IDord-507d173240f34f1caf52bbb6a8580fda
Source noteuspto-grants-2000_03