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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519936Generated: November 3, 2026

3,4-Dibromo-2-nitrothiophene → 2-(4-Bromo-2-nitrothiophen-3-yl)oxazole

https://huagongshe.com/reaction/1519936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dibromo-2-nitrothiopheneHCID 1201506—
Reactant2-(Tri-n-butylstannyl)oxazoleHCID 15486183—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product2-(4-Bromo-2-nitrothiophen-3-yl)oxazoleHCID 6875530767%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3,4-dibromo-2-nitrothiophene (0.166 mg, 0.581 mmol), Pd(PPh3)4 (67 mg, 0.0581 mmol) and 2-(tributylstannyl)oxazole (250 mg, 0.698 mmol) in DMF (1.1 mL) was evacuated and purged with nitrogen three times. The reaction mixture was heated to 90° C. for 18 h and the resulting solution was cooled to room temperature and diluted with Et2O. The solution was washed with brine and the organic phase was separated, dried (Na2SO4), filtered, concentrated under vacuum and purified on a silica gel column (eluant hexane/ethyl acetate, 20/1 to 1/1, v/v) to give 2-(4-bromo-2-nitrothiophen-3-yl)oxazole (107 mg, 67%). Retention time (min)=1.948, method [1], MS(ESI) 274.9 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073891B2
Source datasetuspto-grants-2015_07
ORD IDord-60af20f14a4d4b0f9e0edaaa253db1ac
Source noteuspto-grants-2015_07