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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501796생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/501796

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물CyclopentanoneHCID 8452—
반응물1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
반응물MagnesiumHCID 5462224—
반응물Ammonia chlorideHCID 20976574—
용매Diethyl EtherHCID 3283—
생성물1-(3-(Benzyloxy)phenyl)cyclopentanolHCID 23021569—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772285B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-19059c6449ff4f93ae4008210309f040
출처 메모uspto-grants-2010_08