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HRID 280240作成日:2026年10月25日

Toluene → N-(2-(2,4,6-Trichlorophenoxy)ethyl)-1-propanamine

https://huagongshe.com/reaction/280240

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物(Dimethyl sulfide)trihydroboronHCID 12423031—
反応物N-(n-propyl)-2,4,6-trichlorophenoxyacetamideHCID 13488356—
溶媒MethanolHCID 887—
生成物N-(2-(2,4,6-Trichlorophenoxy)ethyl)-1-propanamineHCID 3842173—

反応条件

温度60 °C

反応手順

N-(n-propyl)-2,4,6-trichlorophenoxyacetamide, 44.0 gm, was added to 250 ml of toluene. 28 ml of borane methyl sulfide [BH3.(CH3)2S] (2 equivalents) was then slowly added to the system. The system was heated at approximately 60° C. for 15 hours at which time reaction completion was checked by IR spectroscopy. 200 ml of methanol was then slowly added to the system. After addition of the methanol, the system was acidified by bubbling in HCl gas. Afterwards, the system was refluxed for 1 hour. The solvent was then removed by stripping. The resulting oil was dissolved in methanol which was then stripped. The oil was next dissolved in methylene chloride. The organic solution was washed with a sodium hydroxide solution and then with water. The methylene chloride was removed by stripping to give 36.3 gm of the N-(n-propyl)ethanolamine 2,4,6-trichlorophenylether, as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04588735
出典データセットuspto-grants-1986_05
ORD IDord-684ecec84dac45e2b6c71a48617ca3a5
出典メモuspto-grants-1986_05