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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749004Generated: October 31, 2026

Ethyl Acrylate → HCID 89843276, compound

https://huagongshe.com/reaction/1749004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantN-Methyl dicyclohexylamineHCID 24210—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantHCID 21209133HCID 21209133—
Catalysttrans-Bis(acetato)bis[2-[bis(2-methylphenyl)phosphino]benzyl]dipalladium(II)HCID 11104995—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 89843276HCID 89843276—

Reaction Steps

The target solid of step 1 (4 g, 14.78 mmol), Herrmann's palladacycle (0.277 g, 0.30 mmol), and [(t-Bu)3Ph]BF4 (0.171 g, 0.60 mmol) mixed in DMF (40 mL) was added with ethyl acrylate (1.58 mL, 14.76 mmol) and Cy2NMe (3.27 mL, 14.78 mmol) and irradiated with microwave at 150° C. for 30 min (two times). The resulting mixture was evaporated to get dark green residue. The residue was suspended in ethyl acetate (50 mL) and washed with water (3×50 mL). The organic layer dried over MgSO4 was evaporated to get crude yellow solid of target compound of step 2. The yellow solid was put to step 3 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09155739B2
Source datasetuspto-grants-2015_10
ORD IDord-ff87fa86d9834e04b1171db47d62174e
Source noteuspto-grants-2015_10