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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197604Generated: October 29, 2026

Methyl vinyl ketone → 4-(3-Chloropyridin-2-yl)-4-methylcyclohex-2-enone

https://huagongshe.com/reaction/2197604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl vinyl ketoneHCID 6570—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(3-Chloropyridin-2-yl)propanalHCID 86630283—
SolventDiethyl EtherHCID 3283—
Product4-(3-Chloropyridin-2-yl)-4-methylcyclohex-2-enoneHCID 6749994922%

Reaction Steps

To a 0° C. solution of the product of Example 38D (0.71 g, 4.19 mmol) in diethyl ether (10 mL) was added a solution of potassium hydroxide (3M in methanol, 0.56 mL, 1.68 mmol), followed by methyl vinyl ketone (0.47 g, 0.55 mL, 6.70 mmol). The reaction was allowed to warm to ambient temperature and stirred overnight. The reaction mixture was diluted with diethyl ether, and washed with water and brine. The organic layer was concentrated, and the residue was chromatographed on silica gel eluting with 25% ethyl acetate-hexane to give the title compound (0.20 g, 22%). 1H NMR (300 MHz, DMSO-d6) δ ppm 8.53 (dd, J=1.5, 4.6, 1H), 7.92 (dd, J=1.5, 8.0, 1H), 7.45-7.26 (m, 2H), 5.92 (d, J=10.2, 1H), 2.82-2.67 (m, 1H), 2.64-2.52 (m, 1H), 2.31 (ddd, J=4.8, 7.2, 17.3, 1H), 2.12-2.00 (m, 1H). MS (DCI) m/z 222 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338603B2
Source datasetuspto-grants-2012_12
ORD IDord-79ba0d517b3746b0bd21f75fffc77a6a
Source noteuspto-grants-2012_12