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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29131생성일: 2026년 10월 25일

Nitric Acid → 2-Bromo-2-(3-hydroxyadamantan-1-yl)acetic acid

https://huagongshe.com/reaction/29131

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Sulfuric AcidHCID 1118—
반응물2-(Adamantan-1-yl)-2-bromoacetic acidHCID 2769715—
용매WaterHCID 962—
생성물2-Bromo-2-(3-hydroxyadamantan-1-yl)acetic acidHCID 3274614—

반응 조건

온도28 °C

반응 단계

α-Bromotricyclo[3.3.1.13,7]decane-1-acetic acid (Formula O) is then reacted with H2SO4 and HNO3 to produce α-bromo-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula Q). More specifically, α-bromo-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula Q) is prepared from α-bromotricyclo[3.3.1.13,7]decane-1-acetic acid (Formula O) by first charging an Erlen-Meyer flask with H2SO4. The flask is then cooled in an ice bath and 50% HNO3 is added to the flask. The solid α-bromotricyclo[3.3.1.13,7]decane-1-acetic acid (Formula O) is then added to the mixture in portions which maintain the temperature under 28° C. The reaction is then heated to 60° C. with stirring until a clear solution is obtained. When the reaction is complete, it is cooled to and maintained at room temperature. Water is then added to quench the reaction. The resulting slurry is cooled in an ice bath and then filtered to obtain α-bromo-3-hydroxytricyclo [3.3.1.13,7]decane-1-acetic acid (Formula Q). See also Example 18 herein.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420079B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-cfb2860a59194e57b88e49052db281d3
출처 메모uspto-grants-2008_09