戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 466643作成日:2026年10月24日

3-Bromobenzaldehyde → 1-Bromo-3-(2-methyl-1-propenyl)benzene

https://huagongshe.com/ja/reaction/466643

反応式

関与物質

役割名称HCID仕込み量
反応物3-BromobenzaldehydeHCID 76583—
反応物Isopropyltriphenylphosphonium iodideHCID 2723783—
反応物Potassium tert-butoxideHCID 23665647—
触媒18-Crown-6HCID 28557—
溶媒TetrahydrofuranHCID 8028—
生成物1-Bromo-3-(2-methyl-1-propenyl)benzeneHCID 2170683675.3%

反応手順

To a stirred slurry of 17.83 g (41.2 mmol) of isopropyltriphenylphosphonium iodide and 300 mg (1.1 mmol) of 18-crown-6 in 50 mL of THF under nitrogen at 5° C. was added 4.60 g (41.0 mmol) of potassium t-butoxide over 5 minutes. The resulting deep red-orange slurry was stirred 10 minutes and then a solution of 4.31 mL (37.0 mmol) of 3-bromobenzaldehyde in 40 mL of THF was added at a rate to keep the temperature below 10° C. The resulting bright yellow slurry was stirred for 20 minutes and then poured into 300 mL of hexanes. The solids were filtered off and the filtrate evaporated. This residue was purified by flash chromatography (5×15 cm column) and eluted with hexanes to provide 5.88 g (75%) of title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05157027
出典データセットuspto-grants-1992_10
ORD IDord-2e4bd4a7bf1b4401a81feba32fb102f2
出典メモuspto-grants-1992_10