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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524413Generated: October 26, 2026

N-bromobutanimide → Ethyl 3-bromo-4-oxocyclohexane-1-carboxylate

https://huagongshe.com/reaction/524413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 4-oxocyclohexanecarboxylateHCID 317638—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
ProductEthyl 3-bromo-4-oxocyclohexane-1-carboxylateHCID 12917737140.8%

Reaction Steps

To a stirred solution of N-bromosuccinimide (1.11 g, 6.274 mmol), PTSA (0.108 g, 0.627 mmol) in toluene (15 mL) was added 4-oxocyclohexanecarboxylic acid ethyl ester (1.068 g, 6.274 mmol) under nitrogen atmosphere and the reaction was refluxed for 2 hrs. Toluene was evaporated under reduced pressure and the residue was partitioned between water (50 mL) and ethyl acetate (50 mL). The layers were separated; the organic layer was washed with sat. sodium bicarbonate solution followed by brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to get title the compound (2.2 g) which was carried without purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340506B2
Source datasetuspto-grants-2016_05
ORD IDord-32c34edfc985463ca8545d3fd3a48dc1
Source noteuspto-grants-2016_05