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HRID 379640作成日:2026年10月26日

1-(Chloromethyl)-4-(methylthio)benzene → 2-Methyl-3-(4-methylthiobenzyl)-1-indanone

https://huagongshe.com/reaction/379640

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Chloromethyl)-4-(methylthio)benzeneHCID 70128—
反応物2-MethylindanoneHCID 249262—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methyl-3-(4-methylthiobenzyl)-1-indanoneHCID 18367456—

反応手順

To a cooled solution (−70° C.) of LDA (1 M) in THF (37 mL) was added dropwise a solution of 2-methyl-1-indanone (J.A.C.S. Vol. 98, 8119-8124 (1976)) (2.5 g, 17 mmol) in THF (20 mL). The resulting dark red solution was stirred at room temperature for 3 hours, then cooled to −20° C. and a solution for 4-methylthiobenzyl chloride (3.1 g, 18 mmol) in THF (15 mL) was added slowly. The addition completed, the reaction mixture was stirred at −20° C. for 30 minutes before being quenched with 3N aqueous HCl (50 mL) and brine (50 mL). The product was extracted with ether, dried over MgSO4 and evaporated to dryness. The oily residue was chromatographed on silica gel eluting with a 1:5 mixture of ethyl acetate-hexane to afford the pure title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06300346B1
出典データセットuspto-grants-2001_10
ORD IDord-6e463c8082fe4fbbbdd06b9eff4ef69d
出典メモuspto-grants-2001_10