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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748615Generated: October 31, 2026

Sodium Carbonate → 4-(5-Bromo-3-methylpyridin-2-yl)cyclohex-3-en-1-one

https://huagongshe.com/reaction/1748615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-3-methylpyridineHCID 86692475—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product4-(5-Bromo-3-methylpyridin-2-yl)cyclohex-3-en-1-oneHCID 8669256045.6%

Reaction Steps

5-Bromo-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-3-methylpyridine (21.1 g) described in Reference Example 105 was dissolved in concentrated hydrochloric acid (64.5 ml) and water (64.5 ml), and stirred at room temperature. After completion of the reaction, the reaction solution was ice-cooled, 10% sodium carbonate aqueous solution was added thereto to adjust the solution to pH 8, the precipitated solid was collected by filtration, washed with water, and then dried under air blow. The obtained solid was dissolved in ethanol, and the solvent was evaporated. This procedure was repeated twice, then to the obtained residue were added n-hexane and a small amount of ethyl acetate, washed, collected by filtration, and heat-dried in vacuo to give 4-(5-bromo-3-methylpyridin-2-yl)cyclohex-3-en-1-one (8.26 g) as a pale yellow solid. MS (ESI) m/z: 266, 268 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-51a4ec77fd8444868fef9673246fad42
Source noteuspto-grants-2015_10