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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190393Generated: October 27, 2026

3-(1-cyano-1-methylethyl)-N-[3-(4-nitrophenoxy)phenyl]benzamide → N-[3-(4-aminophenoxy)phenyl]-3-(1-cyano-1-methylethyl)benzamide

https://huagongshe.com/reaction/2190393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-cyano-1-methylethyl)-N-[3-(4-nitrophenoxy)phenyl]benzamideHCID 57386826—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-(4-aminophenoxy)phenyl]-3-(1-cyano-1-methylethyl)benzamideHCID 5738682798%

Reaction Steps

To a solution of 3-(1-cyano-1-methylethyl)-N-[3-(4-nitrophenoxy)phenyl]benzamide (8.10 g, 20.2 mmol) in tetrahydrofuran (50 mL) and methanol (50 mL) was added 10% palladium-carbon (555 mg), and the mixture was stirred under a hydrogen atmosphere (2.5 atm) at room temperature for 14 hr. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (7.34 g, 98%) as a pale-gray amorphous substance. The obtained compound was used in the next reaction without a further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324395B2
Source datasetuspto-grants-2012_12
ORD IDord-2e08fdc4a94f463d8bcdccd551979ead
Source noteuspto-grants-2012_12