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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934514Generated: October 26, 2026

2-Methylcyclohexanone → 2-Bromo-2-methylcyclohexanone

https://huagongshe.com/reaction/1934514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylcyclohexanoneHCID 11419—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-2-methylcyclohexanoneHCID 11116853100%

Reaction Steps

A solution of 15 g (0.134 mol) of 2-methyl-1-cyclohexanone (7) and 23.84 g (0.134 mol) of N-bromosuccinimide in 150 mL of carbon tetrachloride was stirred and heated to reflux for 12 h under argon. The mixture was cooled to room temperature, filtered through Celite to remove succinimide and the filter cake was washed with 150 mL of ether. The filtrate was concentrated to give 25.6 g (100% yield) of 2-bromo-2-methyl-1-cyclohexanone. 1H NMR δ3.21 (td, J=16 Hz, 8 Hz, 1H, CH—CO), 2.36 (m, 2H), 2.06 (m, 2H), 1.82 (s, 3H, Me), 1.77 (m, 2H), 1.62 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384045B1
Source datasetuspto-grants-2002_05
ORD IDord-36c43c07512f47b49a06e94b902f7d76
Source noteuspto-grants-2002_05