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HRID 29131作成日:2026年10月25日

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

https://huagongshe.com/reaction/29131

反応式

関与物質

役割名称HCID仕込み量
反応物Nitric AcidHCID 944—
反応物Sulfuric AcidHCID 1118—
反応物2-(Adamantan-1-yl)-2-bromoacetic acidHCID 2769715—
溶媒WaterHCID 962—
生成物2-Bromo-2-(3-hydroxyadamantan-1-yl)acetic acidHCID 3274614—

反応条件

温度28 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420079B2
出典データセットuspto-grants-2008_09
ORD IDord-cfb2860a59194e57b88e49052db281d3
出典メモuspto-grants-2008_09