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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090863Generated: November 1, 2026

2,3,4-Trifluoro-1-nitro-5-(trifluoromethyl)benzene → HCID 15614237, compound

https://huagongshe.com/reaction/1090863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-Trifluoro-1-nitro-5-(trifluoromethyl)benzeneHCID 15614236—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15614237HCID 1561423787.9%

Reaction Steps

35 g of 2,3,4-trifluoro-5-nitro-benzotrifluoride in 150 ml of tetrahydrofuran were initially introduced into a hydrogenation apparatus, 3 g of Raney nickel were added and, after flushing with nitrogen, the mixture was hydrogenated to constant pressure with 30 bar of hydrogen at 25° to 45° C. After completion of the hydrogen uptake, the pressure was released and the reaction solution was filtered and subsequently fractionally distilled. 27 g of 2,3,4-trifluoro-5-amino-benzotrifluoride were obtained with a boiling point of 82° to 83° C. at 15 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082971
Source datasetuspto-grants-1992_01
ORD IDord-2cdd080e605843298aca1d905ea8d5da
Source noteuspto-grants-1992_01