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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914516Generated: November 1, 2026

1,2-Dimethoxyethane → HCID 2783407, compound

https://huagongshe.com/reaction/1914516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
Reactant3'-BromoacetophenoneHCID 16502—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 2783407HCID 278340788.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-(3-bromo-phenyl)-ethanone (4.9 g, 24 mmol), 4-trifluoromethyl phenyl boronic acid (4.6 g, 24 mmol), tetrakis(triphenylphosphine)palladium(0) (1.4 g, 1.2 mmol), potassium phosphate (10 g, 49 mmol), 1,2-dimethoxyethane (50 mL) and water (10 mL) was heated to 80° C. under a blanket of nitrogen in a sealed tube. After 5 h, the mixture was partitioned between water (50 mL) and ethyl acetate (50 mL). The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated. The residue was purified directly by FCC to afford a clear oil (5.6 g, 87%). MS (ESI): mass calcd. for C15H11F3O, 264.0; m/z found, 265.1 [M+H]+. 1H NMR (500 MHz, CDCl3) δ 8.21 (t, J=1.6, 1H), 8.04-7.98 (m, 1H), 7.85-7.78 (m, 1H), 7.76-7.69 (m, 4H), 7.60 (t, J=7.7, 1H), 2.68 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614201B2
Source datasetuspto-grants-2013_12
ORD IDord-f1ba781aa69f4fe9ad987ce3ab65e9c7
Source noteuspto-grants-2013_12