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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63251Generated: October 26, 2026

1-Adamantanecarboxylic acid → 3-Bromoadamantane-1-carboxylic acid

https://huagongshe.com/reaction/63251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Adamantanecarboxylic acidHCID 13235—
ReactantBromineHCID 24408—
ReactantSodium PyrosulfiteHCID 656671—
ReactantAluminum(III) ChlorideHCID 6451240—
Product3-Bromoadamantane-1-carboxylic acidHCID 3081892.83%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A two-neck round bottom flask was connected to a reflux condenser, to which aluminum chloride (AlCl3, 7.15 mmol) was injected, followed by cooling at −5° C. in argon environment. Then, bromine (Br2, 66 mmol) was added thereto, followed by stirring for 15 minutes. 1-adamantanecarboxylic acid (5.5 mmol) was added to the reaction mixture at a time, followed by stirring for 1 hour with maintaining the temperature at −5° C. The reaction mixture was then additionally stirred for 48 hours with raising the temperature slowly to room temperature. Upon completion of stirring, ice water was poured to the mixture to terminate the reaction. Excessive bromine was de-colored by adding sodium pyrosulfite. The de-colored reactant was extracted by using chloroform. The extracted organic layer was dried over sodium sulfate, followed by concentration under reduced pressure to give the target compound (5.016 mmol, 92.83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447063B2
Source datasetuspto-grants-2016_09
ORD IDord-adc2ba3d385e494b94f6a36ac18a0cc8
Source noteuspto-grants-2016_09