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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060946Generated: October 25, 2026

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

https://huagongshe.com/reaction/2060946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
Reactant2-(Adamantan-1-yl)-2-bromoacetic acidHCID 2769715—
Product2-Bromo-2-(3-hydroxyadamantan-1-yl)acetic acidHCID 3274614—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278462B2
Source datasetuspto-grants-2012_10
ORD IDord-bea05f470c464ce89f14e831773db314
Source noteuspto-grants-2012_10