HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451794Generated: October 25, 2026
Acetyl bromide → 1-Bromobicyclo(2.2.2)octane
https://huagongshe.com/reaction/451794
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | Bicyclo[2.2.2]octane, 1-methoxy- | HCID 139061 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Bromobicyclo(2.2.2)octane | HCID 139060 | 75.5% |
Reaction Steps
To a stirred mixture of 1-methoxybicyclo[2.2.2]octane (4.0 g, 28 mmol) and acetyl bromide (6.2 g, 50.4 mmol) was added 10 drops of stannic chloride at 0° C. After stirring for 0.5 h, the temperature was allowed to rise to 20-25° C. and stirring was continued at the same temperature for 3 h. After cooling to 0° C., water (30 mL) was added and the mixture was stirred for 10 min. Then the mixture was poured into water (150 mL) and extracted with ether (100 mL×3). The ether layers were combined, washed with aqueous sodium bicarbonate and water, and dried over sodium sulfate. The solvent was removed under reduced pressure to produce 1-bromobicyclo[2.2.2]octane (4.0 g, 75%), which was used for next step without purification. 1H NMR (CDCl3) δ 2.23 (m, 6H), 1.95 (m, 1H), 1.81-1.63 (m, 6H), 1.52 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487108B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-acc71d7fc0854810b99d7a7769d070f4 |
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| Source note | uspto-grants-2013_07 |
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