Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62665Generated: October 26, 2026

Potassium Carbonate → tert-Butyl 2-nitro-4-(thiophen-2-yl)phenylcarbamate

https://huagongshe.com/reaction/62665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactanttert-Butyl (4-bromo-2-nitrophenyl)carbamateHCID 52904808—
CatalystHCID 178418397HCID 178418397—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Producttert-Butyl 2-nitro-4-(thiophen-2-yl)phenylcarbamateHCID 5973698473%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of tert-butyl (4-bromo-2-nitrophenyl)carbamate (6.0 g, 18.92 mmol, 1.0 eq.), thiophen-2-ylboronic acid (3.2 g, 24.6 mmol, 1.3 eq.), potassium carbonate (7.84 g, 56.8 mmol, 3.0 eq.) and tetrakis(triphenylphosphine)palladium(0) (1.53 g, 1.32 mmol, 0.07 eq.), tri-tolylphosphine in DME/H2O (105 mL) was first degassed then heated to 90° C. for 20 h. The reaction was then filtered through Celite. The product was extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by flash column chromatography (silica gel, 2% EtOAc/hexanes) to obtain pure tert-butyl (2-nitro-4-(thiophen-2-yl)phenyl)carbamate (4.42 g, 73% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447030B2
Source datasetuspto-grants-2016_09
ORD IDord-178d9db47d9a475eb399a78fb53ec9fe
Source noteuspto-grants-2016_09