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HRID 501796作成日:2026年10月25日

Iodine → 1-(3-(Benzyloxy)phenyl)cyclopentanol

https://huagongshe.com/reaction/501796

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物CyclopentanoneHCID 8452—
反応物1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
反応物MagnesiumHCID 5462224—
反応物Ammonia chlorideHCID 20976574—
溶媒Diethyl EtherHCID 3283—
生成物1-(3-(Benzyloxy)phenyl)cyclopentanolHCID 23021569—

反応手順

1.85 g of magnesium was suspended in 15 mL of diethyl ether, to which a catalytic amount of iodine was added and then a solution of 20.00 g of 1-(benzyloxy)-3-bromobenzene in 40 mL of diethyl ether was added dropwise and this mixture was stirred for 8 hours while heating it under reflux. The reaction mixture was cooled to 5° C., to which a solution of 6.72 mL of cyclopentanone in 20 mL of diethyl ether was added dropwise, and this mixture was stirred for one hour at room temperature. Then an aqueous solution of ammonia chloride was added to the ice-cooled reaction mixture, and the organic phase was separated therefrom. After the resultant organic phase was washed with water and a saturated sodium chloride solution successively, the washed phase was dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure. The resultant residue was purified by silica gel column chromatography [eluent; hexane:ethyl acetate=10:1] to yield 7.65 g of 1-[3-(benzyloxy)phenyl] cyclopentanol as yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772285B2
出典データセットuspto-grants-2010_08
ORD IDord-19059c6449ff4f93ae4008210309f040
出典メモuspto-grants-2010_08