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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1,1-Trifluoro-4-methylpent-3-en-2-one | HCID 22032691 | — |
| Reactant | HCID 178489560 | HCID 178489560 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 46938919 | HCID 46938919 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579469B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-45c828f16c204209860bb6dc53a916f4 |
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| Source note | uspto-grants-2009_08 |
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