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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 618479생성일: 2026년 10월 24일

Water → 7-(1-Adamantyl)-6-benzyloxy-2-bromonaphthalene

https://huagongshe.com/ko/reaction/618479

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물3-(Adamantan-1-yl)-6-bromonaphthalen-2-olHCID 14549072—
용매EthanolHCID 702—
용매DimethylformamideHCID 6228—
생성물7-(1-Adamantyl)-6-benzyloxy-2-bromonaphthaleneHCID 22000359—

반응 단계

1.26 g (42 mmol) of sodium hydride (80% in oil) and 50 ml of DMF were introduced into a 3-necked flask, a solution of 12.5 g (35 mmol) of 7-(1-adamantyl)-6-hydroxy-2-bromonaphthalene in 100 ml of DMF was added dropwise and stirring was carried out until gas evolution had ceased. 5 ml (42 mmol) of benzyl bromide were then added and stirring was carried out at room temperature for 2 hours. The reaction mixture was poured into water and extracted with ethyl ether and the organic phase was separated by settling, dried over magnesium sulfate and evaporated. The residue obtained was taken up in ethanol, heated to reflux, cooled, filtered and dried. 12.5 g (80%) of the expected compound were collected, which compound had a melting point of 150°-1° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05952382
출처 데이터셋uspto-grants-1999_09
ORD IDord-3d5c682f50c74932bc97b777b9476532
출처 메모uspto-grants-1999_09