Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467911Generated: October 26, 2026

Iodine → ethyl 2-(3,5-dimethyl-1H-pyrazol-1-yl)propanoate

https://huagongshe.com/reaction/1467911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant3,5-DimethylpyrazoleHCID 6210—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-bromopropionateHCID 79040—
SolventAcetonitrileHCID 6342—
Productethyl 2-(3,5-dimethyl-1H-pyrazol-1-yl)propanoateHCID 1200867571.2%

Reaction Steps

A suspension of 3,5-dimethyl-1H-pyrazole (ALDRICH, 8 g, 0.083 mol), anhydrous K2CO3 (ALDRICH, 11.50 g, 0.083 mol) and ethyl 2-bromopropanoate (ALDRICH, 15 g, 0.083 mol) in 50 mL of dry ACN was refluxed with mechanical stirring for 24 h. Reaction was checked by TLC (iodine), and starting material was detected. 0.2 equivalents of K2CO3 were added to the mixture which was refluxed over the weekend. Reaction was checked, starting material was still detected. 0.2 eq. of K2CO3 were added to the mixture, which was refluxed during 24 additional hours. Reaction mixture was filtered. Solvent was evaporated under reduced pressure. Residue was diluted with 50 ml of DCM, and washed with water. Organic layer was separated and aqueous fraction was extracted three times with 70 mL of DCM. Combined organic extracts were washed with brine, dried over Na2SO4 (anh), filtered and concentrated under reduce pressure. Residue was purified using a 70 g silica gel cartridge with a linear gradient of hexane/EtOAc 100/0 to 20/80 to yield the title compound (11.6 g 71%) as colourless oil. 1H NMR (300 MHz, CDCl3) δ ppm: 5.83 (s, 1H), 4.85 (q, 1H), 4.08-4.25 (m, 2H), 2.22-2.23 (m, 6H), 1.79 (d, 3H), 1.23 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000181B2
Source datasetuspto-grants-2015_04
ORD IDord-884d69f39b094673bed870d8e00f6d25
Source noteuspto-grants-2015_04