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HRID 269454作成日:2026年10月26日

Hydrochloric Acid → 2-Bromo-4-isopropylaniline

https://huagongshe.com/reaction/269454

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4-IsopropylanilineHCID 7464—
反応物Acetic AnhydrideHCID 7918—
反応物Potassium HydroxideHCID 14797—
反応物BromineHCID 24408—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物2-Bromo-4-isopropylanilineHCID 521337—

反応条件

温度50 °C

反応手順

A mixture of 99 g (0.73 mol) of 4-isopropylaniline (Acros) and 300 ml of acetic acid was refluxed for 1 h; then, 75 g of acetic anhydride was added dropwise while vigorously stirring. The resulting solution was cooled to 50° C., and 37.4 ml of bromine was added dropwise, while vigorously stirring, over ca. 30 min. Then, 370 ml of 12 M HCl was added and this mixture was refluxed until a precipitate was formed. This precipitate was separated, washed with 2×150 ml of methyl-tert-butyl ether, and dried in vacuum. A mixture of the solid obtained and a solution of 112 g of KOH in 300 ml of water was stirred at 50-60° C. for 1 h. The organic layer was separated, and the aqueous layer was extracted with 2×150 ml of methyl-tert-butyl ether. The combined extract was dried over K2CO3 and evaporated to dryness. Fractional distillation gave the title product, b.p. 107-111° C./3 mm Hg. Yield 83.7 g (77%) of yellowish oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07446216B2
出典データセットuspto-grants-2008_11
ORD IDord-f9534332412b40a08b2ab7d09c5ad8b9
出典メモuspto-grants-2008_11