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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169997Generated: October 27, 2026

Sodium Carbonate → 2-Nitro-4-(thiophen-2-yl)aniline

https://huagongshe.com/reaction/1169997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromobenzene-1,2-diamineHCID 323593—
Reactant2-Thiopheneboronic acidHCID 2733960—
ReactantN,N-Dimethylformamide--water (1/1)HCID 21962138—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
Product2-Nitro-4-(thiophen-2-yl)anilineHCID 22664831—

Reaction Conditions

Temperature23 °C

Reaction Steps

4-Bromobenzene-1,2-diamine (1.0 equivalent) and Na2CO3 (2.0 equivalents) were dissolved in DMF/H2O (5:1) at room temperature. Nitrogen was bubbled through the reaction mixture for 5 minutes and PdCl2(dppf)2 (0.1 equivalents) was added. After stirring at 23° C. for approximately 10 minutes, 2-thiopheneboronic acid (1.1 equivalents) in DMF was added and the reaction was heated at 90° C. for 12 hours. After this time, the solution was concentrated and partitioned between EtOAc and H2O. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4 and concentrated under reduced pressure. The resulting black residue was purified by silica gel chromatography (0-20% EtOAc:hexanes) to yield an orange solid. LC/MS m/z 221.1 (MH+), Rt 2.67 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825132B2
Source datasetuspto-grants-2010_11
ORD IDord-a124d9feabac434dae00539a01851acf
Source noteuspto-grants-2010_11