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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508658Generated: October 28, 2026

Ethyl Acrylate → ethyl(E)-3-(3-chloro-6-pyridazinyl)-2-propenoate

https://huagongshe.com/reaction/508658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant3-Chloro-6-iodopyridazineHCID 15418839—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDiisopropylethylamineHCID 81531—
Productethyl(E)-3-(3-chloro-6-pyridazinyl)-2-propenoateHCID 532594108.2%

Reaction Conditions

Temperature111 °C

Reaction Steps

A suspension of 3-chloro-6-iodopyridazine (2.4 g, 10 mmol), ethyl acrylate (4.4 mL, 40 mmol), palladium(II) acetate (90 mg, 0.40 mmol) and tri(o-tolyl)phosphine (366 mg, 1.20 mmol) in DMF (10 mL) and diisopropylethyl amine (5 mL) was stirred with heating (111° C. oil-bath) for 3.5 h, cooled to room temperature, diluted with H2O (50 mL) and extracted with EtOAc (300 mL). The extract was washed (brine) and dried. After solvent removal at reduced pressure, the residue was chromatographed (14% to 20% EtOAc/hexane) to give 174 mg (8%) of ethyl(E)-3-(3-chloro-6-pyridazinyl)-2-propenoate as a brown solid, mp 106-110° C. IR 2928, 1715, 1186 cm−1; 1H NMR (CDCl3) δ 1.38 (t, J=7.5 Hz, 3H, CH2CH3), 4.33 (q, J=7.5 Hz, 2H, CH2CH3), 7.98 (d, J=16.2 Hz, 1H, CH═CHCO), 7.57 (d, J=8.4 Hz, 1H, 4-ArH), 7.63 (d, J=8.4 Hz, 1H, 5-ArH), 7.86 ppm (d, J=16.2 Hz, 1H, CH═CHCO). HRMS calcd C9H9ClN2O2 [M+H]+ 213.0425. found 213.0431.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096544B2
Source datasetuspto-grants-2015_08
ORD IDord-25d58a3420ed474c929dd5f616a3bcc3
Source noteuspto-grants-2015_08