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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173150Generated: October 26, 2026

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

https://huagongshe.com/reaction/1173150

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, 9H), 8.58 (d, J=8.8 Hz, 1H), 8.39 (d, J=2.1 Hz, 1H), 7.81 (dd, J=8.8, 1.8 Hz, 1H), 7.32 (m, 2H), 7.09 (dd, J=5.3, 3.8 Hz, 1H), 1.54 (s, 9H); MS (ESI+): cal'd [M+Na]+ 343.1, obs'd 343.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834026B2
Source datasetuspto-grants-2010_11
ORD IDord-1270e156fda740d08780739543169b93
Source noteuspto-grants-2010_11