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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595020Generated: October 31, 2026

Aniline → HCID 9817275, compound

https://huagongshe.com/reaction/1595020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTert-Butyl nitriteHCID 10906—
Reactant3,5-DinitroanilineHCID 12068—
Reactant(3-bromoprop-1-en-2-yl)benzeneHCID 234998—
SolventAcetonitrileHCID 6342—
ProductHCID 9817275HCID 981727535.2%

Reaction Conditions

Temperature25.5 °C

Reaction Steps

To a solution of t-butylnitrite (119 μl, 1.0 mmol) and 2-phenyl-3-brompropene (0.99 g, 5.0 mmol) in CH3CN (0.5 ml) was 3,5-dinitroaniline (92 mg, 0.5 mmol) added during 10 minutes, while maintaining the temperature of the reaction mixture at 23-28° C. At the end of the addition of the aniline extra t-butylnitrite (119 μl, 1.0 mmol) was added to the reaction mixture which then was heated to 35° C. for 5 minutes. The reaction mixture was stirred at 22° C. for one hour. The volatile material in the reaction mixture was removed at reduced pressure. Column chromatography (heptane-ethyl acetate 23:2) succeeded by crystallization from heptane gave 50 mg (35%) of 3,5-dinitro-1-(2-phenyl-2-propenyl)benzene as bright yellow needles. 1H NMR (CDCl3, 400 MHz) δ 8.88, (t, 1H, J=2.1 Hz), 8.42, (d, 2H, J=2.1 Hz), 7.42-7.37, (m, 2H), 7.36-7.24, (m, 3H), 5.65, (s, 1H), 5.22, (d, 1H, J=0.8 Hz), 4.08, (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284894B1
Source datasetuspto-grants-2001_09
ORD IDord-9d3c3deffd4a434a81942aedfc1b0645
Source noteuspto-grants-2001_09