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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736470Generated: October 30, 2026

2-Nitroaniline → HCID 22478779, compound

https://huagongshe.com/reaction/736470

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitroanilineHCID 6946—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 22478779HCID 22478779239%

Reaction Steps

To a mixture of 2-nitroaniline (1.73 g, 12.5 mmol), DMAP (321 mg, 2.6 mmol) and 2,6-di-tert-butyl-4-methylphenol (308 mg) in dry dichloromethane (50 mL) at 0° C. was added triethylamine (10.6 mL, 76 mmol) followed by acryloylchloride (3.2 mL, 38 mmol, 3.0 equiv.), and the mixture was stirred at room temperature for 16 h. The solution was diluted with dichloromethane (250 mL), cooled to 0° C. and the excess of reagent quenched with saturated NaHCO3 (stirring for 1 h). The organic layer was then washed (5% KHSO4, then brine), dried (MgSO4), filtered and concentrated under reduced pressure. After purification through chromatographic column on silica gel (elution 50% ether in hexanes), 642 mg (3.34 mmol, 27% yield) of the amide was obtained. 13C NMR (300 MHz, CDCl3) δ (ppm): 163.6, 136.0, 135.6, 134.5, 131.3, 128.6, 125.4, 123.1, 121.8. LRMS=193.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595343B2
Source datasetuspto-grants-2009_09
ORD IDord-0b7b98fc29b34e5691a91686a9c0c304
Source noteuspto-grants-2009_09