Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133105Generated: October 26, 2026

2-(4-tert-butyl-phenyl)-8-nitro-2H-phthalazin-1-one → 8-amino-2-(4-tert-butyl-phenyl)-2H-phthalazin-1-one

https://huagongshe.com/reaction/133105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-tert-butyl-phenyl)-8-nitro-2H-phthalazin-1-oneHCID 69158867—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product8-amino-2-(4-tert-butyl-phenyl)-2H-phthalazin-1-oneHCID 69160627—

Reaction Steps

A solution of the nitro compound (Step D) and EtOAc (10 mL) was hydrogenated over 10% Pd/C (20 mg) at RT and at atmospheric pressure. After 4 h, the mixture was filtered through Celite® and concentrated in vacuo to afford the desired compound as an orange oil. MS m/e 294 (M+H)+. Calc'd for C18H19N3O: 293.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390820B2
Source datasetuspto-grants-2008_06
ORD IDord-9e0bf932c1e44e1e82edcbe72ba6a7d8
Source noteuspto-grants-2008_06