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HRID 1874作成日:2026年10月23日

Hydrogen Peroxide → 4-t-Butoxy-2,3,6-trifluoro-5-hydroxypyridine

https://huagongshe.com/ja/reaction/1874

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Trimethyl borateHCID 8470—
反応物Sodium HydroxideHCID 14798—
反応物Lithium diisopropylamideHCID 2724682—
反応物4-t-Butoxy-2,3,6-trifluoropyridineHCID 10608547—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
生成物4-t-Butoxy-2,3,6-trifluoro-5-hydroxypyridineHCID 10656587—

反応条件

温度-78 °C

反応手順

A 11.16 g (54.39 mmol) sample of 4-t-butoxy-2,3,6-trifluoropyridine, from Example 253 step b above, was dissolved in 50 mL of THF, and the solution was cooled to -78° C. To this solution was added LDA (65.6 mmol) with stirring for 30 min, during which a solid preciptated. To this mixture was added 7.5 mL of trimethoxyborane, with stirring for 25 min at -78° C. To this mixture was added 10 mL of acetic acid, and the mixture was stirred and allowed to warm to room temperature. Next was added 100 mL of 30% hydrogen peroxide and 100 mL of 2N sodium hydroxide while cooling in an ice bath. The mixture was then stirred at room temperature for 16 hours, and quenched with saturated NH4Cl solution. The mixture was extracted with ether, and the extract was washed with brine and dried over MgSO4. The solvent was removed under vacuum, and the residue was purified by flash chromatography on silica gel, eluting with 1:8 ethyl acetate:hexane. Removal of the solvent gave 9.769 g of the title product as a colorless liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726182
出典データセットuspto-grants-1998_03
ORD IDord-c191750ca7b54fdb8dafaf0853defb9d
出典メモuspto-grants-1998_03