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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Adamantanecarboxylic acid | HCID 13235 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 3-Bromoadamantane-1-carboxylic acid | HCID 30818 | 92.83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447063B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-adc2ba3d385e494b94f6a36ac18a0cc8 |
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| Source note | uspto-grants-2016_09 |
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