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HRID 1420741作成日:2026年10月27日

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

https://huagongshe.com/reaction/1420741

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US06071934
出典データセットuspto-grants-2000_06
ORD IDord-09c34f1f1b574466b1967ef7876d80de
出典メモuspto-grants-2000_06