HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243186Generated: October 27, 2026
Bromine → 2-Bromo-4,4-dimethylcyclohexan-1-one
https://huagongshe.com/reaction/2243186
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Cyclohexanone, 4,4-dimethyl- | HCID 138166 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Bromo-4,4-dimethylcyclohexan-1-one | HCID 20271204 | 78.4% |
Reaction Steps
1.71 g (10.7 mmol) of bromine were added in one portion to a solution of 1.35 g (10.7 mmol) of 4,4-dimethyl-cyclohexanone in methanol (10 ml) at −10° C. The reaction mixture was then stirred for 10 min at −10° C., for 30 min at 0° C. and finally for 8 h at RT. The reaction was then quenched by addition of water (5 ml) and stirred overnight at RT. Additional water was added (20 ml) leading to the formation of a precipitate that was collected by filtration. The crude 2-bromo-4,4-dimethyl-cyclohexanone (1.72 g, 78%) that was obtained as an orange solid was used in the next reaction step without further purification. 1HNMR (CDCl3, 300 MHz): δ 1.09 (s, 3H), 1.23 (s, 3H), 1.75 (m, 2H), 2.09 (t, J=13.1 Hz, 1H), 2.34 (ddd, J=13.3 and 6.1 and 2.8 Hz, 1H), 2.59 (m, 2H), 4.77 (dd, J=12.9 and 5.9 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674815B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-370d56558f054418a17719a18c9db2f9 |
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| Source note | uspto-grants-2010_03 |
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