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HRID 247354作成日:2026年10月27日

N,N-Dimethylaniline → Triethylamine hydrochloride

https://huagongshe.com/reaction/247354

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylanilineHCID 949—
反応物Diethyl EtherHCID 3283—
反応物DichloromethaneHCID 6344—
反応物TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物Triethylamine hydrochlorideHCID 11130—
生成物Benzenamine, N,N-dimethyl-, hydrochloride (1:1)HCID 79987—

反応手順

The aminations of Equations 43a and 43e are most conveniently effected by adding the requisite sulfonyl chlorides to a solution of the aminopyrazoles LIIa and LIIa' in a suitable solvent such as diethyl ether, tetrahydrofuran, or methylene chloride containing at least two equivalents of an acid scavenger such as triethylamine or dimethylaniline at temperatures between 0° C. and 65° C. The desired sulfonamides of Formulas LIIb and LIIb' are isolated either by filtration, in which case the by-product triethylamine hydrochloride or dimethylaniline hydrochloride is removed by washing with water, or extraction into a suitable organic solvent such as methylene chloride or ethyl acetate. Drying and evaporation of the solvent then affords the products LIIb and LIIb', which are usually sufficiently pure to be carried directly onto the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04707178
出典データセットuspto-grants-1987_11
ORD IDord-e8e56736969d488e907e0347c78e394e
出典メモuspto-grants-1987_11