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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602744Generated: November 1, 2026

Acetic Anhydride → HCID 18355491, compound

https://huagongshe.com/reaction/1602744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant(alpha,alpha,alpha-Trifluoro-4-tolyl)acetic acidHCID 118342—
Reactant2,4'-Dihydroxy-4-methoxybenzophenoneHCID 282356—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 18355491HCID 18355491—

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of (2-hydroxy-4-methoxyphenyl)-(4-hydroxyphenyl)-methanone (7.33 g, 30.0 mmol), acetic anhydride (15 ml), triethylamine (5.5 ml, 39.5 mmol), and 4-(trifluoromethyl)phenyl acetic acid (4.63 g, 30.0 mmol) was stirred at 135° C. for 18 h, and the resulting orange coloured solution poured into water (120 ml) and stirred for 3 h. The resulting mixture of aqueous solution plus sticky solid was diluted with ethyl acetate (300 ml) to dissolve the solid, and the organic layer separated. The aqueous phase was further extracted with ethyl acetate (2×100 ml). The combined organic extracts were washed with water, saturated sodium chloride solution, dried over sodium sulfate and evaporated to give a yellow/orange solid, which was recrystallised from 6:1 ethanol/water (350 ml) to give the product as a colourless solid, which was vacuum dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05985306
Source datasetuspto-grants-1999_11
ORD IDord-45ba24995bd5479498ad7dd002ac9cbe
Source noteuspto-grants-1999_11