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HRID 377361作成日:2026年10月26日

Hydrochloric Acid → (Z)-5-Fluoro-3-(2-hydroxyethyl)-2-methyl-1-(4-methylsulfonylbenzylidene)indene

https://huagongshe.com/reaction/377361

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-(Methylsulfonyl)benzaldehydeHCID 220376—
反応物Sodium MethoxideHCID 10942334—
反応物5-fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethaneHCID 13933293—
溶媒MethanolHCID 887—
生成物(Z)-5-Fluoro-3-(2-hydroxyethyl)-2-methyl-1-(4-methylsulfonylbenzylidene)indeneHCID 15860332—

反応手順

5-Fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethane (15 g, 0.072 mol), p-methylsulfonylbenzaldehyde (14.0 g, 0.091 mol) and sodium methoxide (13.0 g, 0.24 mol) are heated in methanol (200 ml) at 60° C. under nitrogen with stirring for 6 hours. The reaction mixture is poured onto ice-water (750 g), and is acidified with 2.5N hydrochloric acid. The collected solid is triturated with a little ether to produce (Z)-5-fluoro-2-methyl-1-(p-methylsulfonylbenzylidene)-1H-3-indenyl-(2-hydroxy) ethane. Recrystallization of the crude reaction product results in the separation of the mixture of geometrical isomers (Z/E) and gives the title compound (R1 =5-fluror, R2 =CH3, R3 =H, R4 =CH2OH, n=1, R5 =CH3SO2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06025394
出典データセットuspto-grants-2000_02
ORD IDord-0c443b68506842a49d541f85a1283d38
出典メモuspto-grants-2000_02