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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432947Generated: October 30, 2026

N-(4-chloro-2-fluoro-5-nitrophenyl)acetamide → N-(5-amino-4-chloro-2-fluorophenyl)acetamide

https://huagongshe.com/reaction/432947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-chloro-2-fluoro-5-nitrophenyl)acetamideHCID 13563753—
SolventEthyl AcetateHCID 8857—
ProductN-(5-amino-4-chloro-2-fluorophenyl)acetamideHCID 1176958495.9%

Reaction Steps

In a 20 L autoclave, 1395 g (6 mole) of N-(4-chloro-2-fluoro-5-nitrophenyl)acetamide and 14 g of Ir-catalyst (5% on carbon, 1% w/w) were suspended in 14 L of ethyl acetate. The autoclave was purged two times with nitrogen at 500 kPa (5 atmospheres) pressure followed by purging with hydrogen at 500 kPa (5 atmospheres). 400 kPa (4 atmospheres) pressure of hydrogen was applied for the hydrogenation and the mixture was heated. At 40° C. hydrogen uptake was accompanied by an exotherm. The temperature was allowed to rise to 75-83° C. The hydrogen uptake was complete after 90 minutes. The reactor was stirred an additional 45 minutes at this temperature and cooled to room temperature. The catalyst was removed by filtration through Celite®. After removal of the solvent at reduced pressure, 1165.5 g of the title compound (95.9%) was obtained as a crystalline solid melting at 142-143° C. (purity: >99.5% by HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664400B2
Source datasetuspto-grants-2003_12
ORD IDord-f33dde45017a4bad917ddebe401ee3f1
Source noteuspto-grants-2003_12