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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106012Generated: October 31, 2026

1,1,1-Trifluoro-4-methylpent-3-en-2-one → HCID 46938919, compound

https://huagongshe.com/reaction/2106012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trifluoro-4-methylpent-3-en-2-oneHCID 22032691—
ReactantHCID 178489560HCID 178489560—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
ProductHCID 46938919HCID 4693891982%

Reaction Steps

To a solution of 2-methoxyphenylmagnesium bromide (131 mL, 65.7 mmol, 0.5M solution in THF) at 0° C. was added CuI (12.5 g, 65.7 mmol). The reaction mixture was warmed to room temperature and stirred for 1 hour. A solution of 4-methyl-1,1,1-trifluoropent-3-en-2-one (10.0 g, 65.74 mmol) (made via procedure in PCT international application WO03/082280, Example 10), in diethyl ether (200 mL) was added and the reaction mixture was stirred overnight. The reaction was quenched with saturated aqueous ammonium chloride (50 mL) and extracted with three 300 mL portions of ethyl acetate. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography using 0%-5% ethyl acetate in hexanes as the eluent. Concentration in vacuo of the product-rich fractions gave 14 g (82%) of 1,1,1-trifluoro-4-(2-methoxyphenyl)-4-methylpentan-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579469B2
Source datasetuspto-grants-2009_08
ORD IDord-45c828f16c204209860bb6dc53a916f4
Source noteuspto-grants-2009_08