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HRID 34603作成日:2026年10月24日

Ethylene Glycol → 1,3-Dioxolane, 2-(3-bromo-4-fluorophenyl)-

https://huagongshe.com/ja/reaction/34603

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物3-Bromo-4-fluorobenzaldehydeHCID 173604—
触媒p-Toluenesulfonic acidHCID 6101—
溶媒TolueneHCID 1140—
生成物1,3-Dioxolane, 2-(3-bromo-4-fluorophenyl)-HCID 1097776578.3%

反応手順

A mixture of 3-bromo-4-fluorobenzaldehyde (45.7 g), ethylene glycol (27.39 g), p-toluenesulphonic acid (0.225 g) and dry toluene (110 cm3) was heated at the reflux temperature under a Dean and Stark trap. After 4.5 hours, approximately 12 cm3 of water had collected in the trap, and analysis of the reaction mixture by gas liquid chromatography indicated that no starting aldehyde was present. The mixture was washed with sodium bicarbonate solution and brine, and dried over anhydrous magnesium sulphate. Evaporation of the solvent under reduced pressure gave a yellow oil, which was purified by distillation under reduced pressure to give 2-(3-bromo-4-fluorophenyl)-1,3-dioxolane (43.56 g), boiling point 68°-106° C. at 0.04 mmHg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04762835
出典データセットuspto-grants-1988_08
ORD IDord-c060ac6cc12e4d48b786ab94b72b761c
出典メモuspto-grants-1988_08