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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340835Generated: October 30, 2026

Ethyl Acrylate → HCID 68415900, compound

https://huagongshe.com/reaction/340835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59332842HCID 59332842—
Catalystpalladium(II) acetateHCID 167845—
SolventPropionitrileHCID 7854—
ProductHCID 68415900HCID 6841590063.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 3-bromo-6,7,8,9-tetrahydro-5-oxa-1,9-diaza-benzocycloheptene (1.1 g, 4.80 mmol), ethyl acrylate (1.5 mL, 14.4 mmol) and diisopropylethylamine (2.5 mL, 14.4 mmol) in propionitrile (100 mL) was purged with an Argon stream for 10 min. Pd(OAc)2 (108 mg, 048 mmol) and P(o-tol)3 (292 g, 0.96 mmol) were added and the Argon purge was repeated. The mixture was stirred at 100° C. for 8 h under Argon. Upon cooling, the resultant mixture was filtered through celite; the filtrate was evaporated. The crude product was purified by chromatography (silica, 0-2% MeOH CH2Cl2) to afford the title compound (0.753 g, 63%). 1H NMR (300 MHz, DMSO-d6, δ): 7.98 (d, J=1.9 Hz, 1H), 7.52 (d, J=1.9 Hz, 1H), 7.51 (d, J=16 Hz, 1H), 6.83 (s, br, 1H), 6.42 (d, J=16 Hz, 1H), 4.15 (m, 4H), 3.34 (m, 2H), 1.98 (m, 2H), 1.25 (t, J=2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895545B2
Source datasetuspto-grants-2014_11
ORD IDord-de908c878e514354826158ba638600a1
Source noteuspto-grants-2014_11