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HRID 78241作成日:2026年10月25日

Acetic Acid → trans-4-Bromo-beta-nitrostyrene

https://huagongshe.com/reaction/78241

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物NitromethaneHCID 6375—
反応物4-BromobenzaldehydeHCID 70741—
反応物Ammonium AcetateHCID 517165—
溶媒WaterHCID 962—
生成物trans-4-Bromo-beta-nitrostyreneHCID 68820483.8%

反応条件

温度100 °C

反応手順

A mixture of 4-bromobenzaldehyde (16.8 g, 91 mmol), nitromethane (24.6 mL, 455 mmol), ammonium acetate (14 g, 182 mmol), and acetic acid (160 mL) was stirred for 4 hours at 100° C. This mixture was cooled to room temperature and poured into water. The precipitate thus produced was collected, washed with water, and dried under a reduced pressure to obtain the title compound (17.4 g). The title compound was used in the following reaction without any further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-047d50064f2148ab898bc3dc70987e87
出典メモuspto-grants-2014_09