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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69866Generated: October 25, 2026

Tert-butyl 1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-4-ylcarbamate → Tert-butyl 1-(2-amino-4-(trifluoromethyl)phenyl)piperidin-4-ylcarbamate

https://huagongshe.com/reaction/69866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-4-ylcarbamateHCID 60507337—
SolventMethanolHCID 887—
ProductTert-butyl 1-(2-amino-4-(trifluoromethyl)phenyl)piperidin-4-ylcarbamateHCID 6904388697%

Reaction Steps

Following the method of Example 49 (Method 2), tert-butyl 1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-4-yl-carbamate in MeOH was reduced yielding tert-butyl 1-(2-amino-4-(trifluoromethyl)phenyl)piperidin-4-ylcarbamate (97%). LCMS (m/z): 360.1 (MH+); LC Rt=3.20 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822497B2
Source datasetuspto-grants-2014_09
ORD IDord-62b28af3e0d04e939848a401b832d409
Source noteuspto-grants-2014_09