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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710449Generated: October 29, 2026

Nitromethane → (E)-2-(1-Admantyl)-1-isopropoxy-4-(2-nitrovinyl)benzene

https://huagongshe.com/reaction/710449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantAmmonium AcetateHCID 517165—
Reactant3-(1-Admantyl)-4-isopropoxybenzaldehydeHCID 87126656—
Product(E)-2-(1-Admantyl)-1-isopropoxy-4-(2-nitrovinyl)benzeneHCID 6672701188%

Reaction Steps

To a stirred solution of 3-(1-admantyl)-4-isopropoxybenzaldehyde (0.24 g, 0.8 mmol) in CH3NO2 (5 mL) was added CH3CO2NH4 (0.125 g, 1.6 mmol) and the mixture was stirred for 3 h at reflux. The solvent was evaporated to dryness and the residue was diluted to 50 ml with EtOAc and washed with 1M HCl and H2O. The organic layer was separated, dried over MgSO4 and filtered. The filtrate was evaporated to dryness to give the title product (0.275 g; 88%) as yellow solid. 1H-NMR (CDCl3) 1.41 (d, 6H, J=6 Hz); 1.7-1.76 (m, 6H); 2.08-2.12 (m, 9H); 4.68-4.74 (m, 1H); 6.85 (d, 1H, J=8.45 Hz); 7.33-7.38 (m, 2H); 7.51 (d, 1H, J=13.53 Hz); 7.97 (d, 1H, J=13.54 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181182B2
Source datasetuspto-grants-2015_11
ORD IDord-16d1f5f7402a4179bb71c6074516d24b
Source noteuspto-grants-2015_11