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HRID 704813作成日:2026年10月23日

p-Toluenesulfonic acid → (E)-1-[3-(4-Chlorophenoxy)phenyl]buten-3-one

https://huagongshe.com/ja/reaction/704813

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Sodium HydroxideHCID 14798—
反応物3-(4-Chlorophenoxy)benzaldehydeHCID 616015—
溶媒AcetoneHCID 180—
溶媒TolueneHCID 1140—
生成物(E)-1-[3-(4-Chlorophenoxy)phenyl]buten-3-oneHCID 20073366—

反応手順

10 N aqu. NaOH (2 ml) was added to a solution of 3-(4-chlorophenoxy)-benzaldehyde (23.3 g, Aldrich) in acetone (150 ml) and stirred vigorously. After a few minutes' stirring, the temperature rose to 32° C. The mixture was left for 5 minutes and then poured into 2 M aqu. HCl (600 ml) and extracted with ether/pet. ether (1:1, 200 ml). The extract was washed with water and satd. aqu. NaCl, dried over MgSO4, and stripped to give the aldol product. The latter was taken up in toluene (300 ml), p-toluenesulphonic acid (1 g) was added, and the mixture heated for 1 hour. The mixture was then cooled, washed with satd. aqu. NaHCO3 and satd. aqu. NaCl, dried over MgSO4 and stripped. The residue was eluted through a slice gel column using methylene chloride/40-60 pet. ether (1:1, followed by 3:1) and the eluate stripped to give the desired product (19 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04988733
出典データセットuspto-grants-1991_01
ORD IDord-b20afd6f017c485282cb258baae5a590
出典メモuspto-grants-1991_01