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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360544Generated: November 1, 2026

Potassium Carbonate → tert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamate

https://huagongshe.com/reaction/2360544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactanttert-Butyl (4-bromo-2-nitrophenyl)carbamateHCID 52904808—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Producttert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamateHCID 57717474—

Reaction Steps

A mixture of tert-butyl (4-bromo-2-nitrophenyl)carbamate (19.4 g, 61.2 mmol), thiophene-2-boronic acid (9.94 g, 77.7 mmol) and K2CO3 (22.2 g, 160 mmol) in 60 mL of dioxane and 60 mL of water was degassed by bubbling nitrogen through the mixture for 30 min. Next, Pd[PPh3]4 (5.25 g, 4.53 mmol) was added and the heterogeneous mixture was warmed to reflux for 20 h. The mixture was cooled and diluted with ethyl acetate, washed with water and brine, dried (MgSO4), and concentrated. The resulting solid was dissolved in diethylether (500 mL) and filtered through a pad of silica. The solvents were removed under reduced pressure to yield the yellow-brown solid: 1H NMR (600 MHz, CDCl3): δ 9.65 (s, 9 H), 8.58 (d, J=8.8 Hz, 1 H), 8.39 (d, J=2.1 Hz, 1 H), 7.81 (dd, J=8.8, 1.8 Hz, 1 H), 7.32 (m, 2 H), 7.09 (dd, J=5.3, 3.8 Hz, 1 H), 1.54 (s, 9 H); MS (ESI+): cal'd [M+Na]+ 343.1, obs'd 343.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686020B2
Source datasetuspto-grants-2014_04
ORD IDord-9d8a53d8f6644c8c9764ce32f12a66f8
Source noteuspto-grants-2014_04