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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907891Generated: November 2, 2026

1-Methylimidazole → 863886-03-7

https://huagongshe.com/reaction/1907891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantButyl AcrylateHCID 8846—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-chloro-N-methyl-2-nitroanilineHCID 258041—
ReactantLithium ChlorideHCID 433294—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylacetamideHCID 31374—
Product863886-03-7HCID 66835685—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a mixture of 4-chloro-2-methylaminonitrobenzene (50.0 g, 268.0 mmol, 1.0 eq), Pd(OAc)2 (0.30 g, 1.3 mmol, 0.005 eq) and LiCl (11.4 g 268.0 mmol, 1.0 eq) in DMAc (250 mL) was added iPr2NEt (56 mL, 321.5 mmol, 1.2 eq) followed by n-butyl acrylate (40 mL, 281.4 mmol, 1.05 eq) under nitrogen. The reaction mixture was stirred at 110° C. for 12 h, then cooled to 50° C. 1-methylimidazole (10.6 mL, 134.0 mmol, 0.5 eq) was added and the mixture was stirred for 30 min before filtering and adding water (250 mL). The resulting mixture was cooled to r.t. over 1 h. The resulting solid was filtered and washed with water and dried to yield n-butyl 3-methylamino-4-nitrocinnamate (71.8 g, 96%, 99.2 A % purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598183B2
Source datasetuspto-grants-2013_12
ORD IDord-d425e3b5424740d19c088e94c7ec6394
Source noteuspto-grants-2013_12