Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534838Generated: October 30, 2026

Methyl 3-nitro-5-(trifluoromethyl)benzoate → methyl 3-amino-5-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/534838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-nitro-5-(trifluoromethyl)benzoateHCID 18942157—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productmethyl 3-amino-5-(trifluoromethyl)benzoateHCID 402678195%

Reaction Steps

A solution of methyl 3-nitro-5-(trifluoromethyl)benzoate (Reference Example 27, 24.6 g, 98.9 mmol) in ethanol (1500 mL) was sparged in a Parr bottle with nitrogen for 10 min. After this time, 10 wt % Pd/C (5.0 g, 5.0 mmol) was added and the reaction mixture was subjected to 40 psi of hydrogen on Parr shaker at room temperature for 1 h. After this time, the reaction mixture was filtered through a pad of celite and concentrated under reduced pressure to provide Methyl 3-amino-5-(trifluoromethyl)benzoate (20.6 g, 95%) as a light purple oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-bfd73034a81045d2bc73a579878aec5f
Source noteuspto-grants-2014_10