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HRID 1648975作成日:2026年10月25日

Propionate ion → Fluazifop-butyl

https://huagongshe.com/reaction/1648975

反応式

関与物質

役割名称HCID仕込み量
反応物Propionate ionHCID 104745—
反応物n-Butyl 2-[4-(5-trifluoromethylpyrid-2-yloxy)phenoxy]acrylateHCID 20481507—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒1-ButanolHCID 263—
生成物Fluazifop-butylHCID 50897—

反応手順

The product (15 g) from Step 3 in n-butanol (300 ml) was hydrogenated at room temperature and atmospheric pressure using a 10% palladium on carbon catalyst. When the uptake of hydrogen ceased, the catalyst was filtered off and the filtrate evaporated under reduced pressure. The residue was purified by short-path distillation (at 140°-150°/0.2 mmHg) to afford a main fraction (11.6 g) containing 57% w/w of the desired propionate which was recrystallised from cold hexane to give n-butyl 2-[4-(5-trifluoromethylpyrid-2-yloxy)-phenoxy]propionate. The propionate may then be obtained substantially pure by recrystallisation from cold hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04414391
出典データセットuspto-grants-1983_11
ORD IDord-e4248a7e14cb4d4ca79cf0131ba920b0
出典メモuspto-grants-1983_11