戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 37585作成日:2026年10月23日

Hydrochloric Acid → 2,2-Difluoro-benzo(1,3)dioxole-4-carbaldehyde

https://huagongshe.com/ja/reaction/37585

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DimethylformamideHCID 6228—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物2,2-Difluoro-1,3-benzodioxoleHCID 74103—
反応物ButyllithiumHCID 178418339—
溶媒TolueneHCID 1140—
生成物2,2-Difluoro-benzo(1,3)dioxole-4-carbaldehydeHCID 2736970—

反応手順

94.0 g (272 mmol) of n-butyllithium (18.5% in toluene) are added dropwise under a nitrogen atmosphere, at from -15° to -10° C., over a period of 1.5 hours, to 29.5 g (254 mmol) of N,N,N',N'-tetramethylethylenediamine and 40.0 g (253 mmol) of 2,2-difluoro-1,3-benzodioxole in 35 ml of toluene, an orange suspension being formed. 19.7 g (270 mmol) of DMF are then metered in at from -15° to -10° C. over a period of 1/2 hour. The pale yellow suspension is poured at +10° C. onto 346 g (1.105 mol) of 11.6% aqueous hydrochloric acid and the whole is stirred for 1/2 hour to complete the reaction. The aqueous phase is separated off and the organic phase is concentrated by evaporation in a vacuum rotary evaporator at 50° C./200 mbar under nitrogen to yield the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420301
出典データセットuspto-grants-1995_05
ORD IDord-3eca32ec96e34b94909277e13a1f16e0
出典メモuspto-grants-1995_05