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HRID 615721作成日:2026年10月24日

Ethyl Bromide → 2-[[2-[4-(4-Trifluoromethylphenoxy)phenoxy]propionyl]]cyclopentane-1,3-dione

https://huagongshe.com/ja/reaction/615721

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物1,3-CyclopentanedioneHCID 77466—
反応物MagnesiumHCID 5462224—
反応物2-{4-[4-(Trifluoromethyl)phenoxy]phenoxy}propanoyl chlorideHCID 12906015—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物2-[[2-[4-(4-Trifluoromethylphenoxy)phenoxy]propionyl]]cyclopentane-1,3-dioneHCID 13309168—

反応手順

Ethyl bromide (6 g, 55 mmol) is added to magnesium turnings (1.34 g) in the presence of tetrahydrofuran (THF; 15 ml). After reaction is complete, the solution is diluted to 50 ml with THF cooled in an ice bath and cyclopentane-1,3-dione (50 mmol) is added rapidly with stirring. THF (250 ml) is added to this mixture and it is allowed to warm to RT. 2-[4-(4-Trifluoromethylphenoxy)phenoxy]propionic acid chloride (55 mmol) is added dropwise with stirring, and the mixture is allowed to stand at RT for 30 minutes. It is then poured into a mixture of ice, water & ether. The aqueous layer is extracted several times with ether. The combined ether extracts are washed with water, dried over sodium sulfate and the solvent is removed to give 2-[[2-[4-(4-trifluoromethylphenoxy)phenoxy]propionyl]]cyclopentane-1,3-dione (V; Y is H, Z is CF3, R1 is CH3 and n is one). ##STR5##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04500737
出典データセットuspto-grants-1985_02
ORD IDord-e59a3cd109da42d59a4add7b43a8dc0e
出典メモuspto-grants-1985_02