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HRID 39332作成日:2026年10月23日

Bromocyclopentane → 4-Cyclopentyloxy-3-hydroxybenzaldehyde

https://huagongshe.com/ja/reaction/39332

反応式

関与物質

役割名称HCID仕込み量
反応物BromocyclopentaneHCID 8728—
反応物3,4-DihydroxybenzaldehydeHCID 8768—
反応物Potassium CarbonateHCID 11430—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物4-Cyclopentyloxy-3-hydroxybenzaldehydeHCID 16726149—

反応条件

温度77.5 °C

反応手順

A suspension of 3,4-dihydroxy benzaldehyde (50.0 g, 0.3623 mol), cyclopentyl bromide (135 g, 0.9058 mol) and potassium carbonate (50.0 g, 0.3623 mol) in N,N-dimethylformamide (500 mL) was stirred at about 75-80° C. for about 1.0 hr. 4×12.5 g potassium carbonate was then added after every 1.0 hr. The reaction mixture was cooled to ambient temperature and filtered to remove inorganic materials. The residue obtained after concentration of the filtrate was diluted with toluene (250 mL), and extracted with 5-10% aqueous sodium hydroxide solution (6×50 mL). The combined aqueous layer was acidified to pH about 3 to 5 by 5N aqueous hydrochloric acid solution. The solid which separated was filtered, washed with water and dried to give 4-cyclopentyloxy-3-hydroxy benzaldehyde.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524905B2
出典データセットuspto-grants-2013_09
ORD IDord-89aa6abc2ce546009d22bfdcfac4be8d
出典メモuspto-grants-2013_09