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HRID 1692364作成日:2026年10月25日

Iodine → 5-Fluoro-2-iodo-4-(trifluoromethyl)phenol

https://huagongshe.com/reaction/1692364

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物ChloroformHCID 6212—
反応物3-Fluoro-4-(trifluoromethyl)phenolHCID 2774800—
触媒Silver trifluoroacetateHCID 76299—
生成物5-Fluoro-2-iodo-4-(trifluoromethyl)phenolHCID 5943649655.7%

反応手順

A solution of iodine (0.874 g, 3.44 mmol) in chloroform (17.1 mL, 214 mmol) was added over a period of 1.5 hours dropwise via addition funnel to a mixture of 3-fluoro-4-(trifluoromethyl)phenol (Preparation 886, 620 mg, 3.4 mmol) and silver trifluoroacetate (0.760 g, 3.44 mmol) in chloroform (3.4 mL, 43 mmol). After addition was complete, the reaction mixture was stirred an additional 1 hour. The reaction mixture was filtered through diatomaceous earth, and the filtrate was washed successively with 10% aqueous sodium thiosulfate (w/v), half-saturated aqueous sodium bicarbonate, water and brine. The organic phase was dried over sodium sulfate, filtered, and concentrated onto diatomaceous earth. The residue was purified by automated flash chromatography (24 g SiO2, hexanes to 1:1 methylene chloride-hexanes gradient elution). The initial product-containing fraction contained predominantly diiodinated material (by mass) with some monoiododinated material. The remaining fractions were concentrated in vacuo to afford the product as a light yellow oil (579 mg, 54%). The product was not dried under vacuum due to volatility.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08153814B2
出典データセットuspto-grants-2012_04
ORD IDord-12a731aeebfa4517a4fc5f6dd886ed0f
出典メモuspto-grants-2012_04