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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220635Generated: October 25, 2026

4-Nitrophenyl formate → tert-Butyl {2-(formylamino)-1-[3-(trifluoromethyl)phenyl]ethyl}carbamate

https://huagongshe.com/reaction/220635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl formateHCID 74628—
Reactanttert-butyl N-{2-amino-1-[3-(trifluoromethyl)phenyl]ethyl}carbamateHCID 43094068—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl {2-(formylamino)-1-[3-(trifluoromethyl)phenyl]ethyl}carbamateHCID 59536815—

Reaction Conditions

Temperature0 °C

Reaction Steps

Of the compound from Example 22A, 75 mg (0.25 mmol) were introduced in 1.5 ml of THF and admixed at 0° C. in small portions with 43.25 mg (0.26 mmol) of 4-nitrophenyl formate. The mixture was stirred at 0° C. for 2 h and then at RT overnight. The solvent was removed on a rotary evaporator and the residue was taken up in DMSO and purified by preparative HPLC (method 10). This gave 66 mg (81% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202895B2
Source datasetuspto-grants-2012_06
ORD IDord-7a916c4c03b0407bb00d937789e968a8
Source noteuspto-grants-2012_06