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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885145Generated: October 31, 2026

Thiophene → HCID 12060894, compound

https://huagongshe.com/reaction/1885145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantIsoamyl NitriteHCID 8053—
Reactant3-BromoanilineHCID 11562—
SolventDiethyl EtherHCID 3283—
ProductHCID 12060894HCID 1206089434%

Reaction Steps

To stirred solution of m-bromoaniline (34.4 g; 0.2M) in thiophene (200 mL) was added isoamylnitrite (46.86 g; 0.4M) dropwise over a period of 30 mins. at 0° C. The resulting mixture was cautiously warmed to R.T. and heated to reflux for 16 hours. The reaction mixture was cooled, diluted with 400 mL of ether, washed with 3×100 mL of satd. sodium chloride solution, and dried over anhydrous magnesium sulfate. Solvent and excess thiophene were removed. A solution of the residue in 200 mL of ether was filtered through 50 G silica gel bed. Solvent was removed, and the residue was distilled to give 34% of 2-(3'-bromophenyl)thiophene as a yellow liquid boiling at 130°-2°/~0.2 mm. This liquid solidified on standing in the refrigerator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05143914
Source datasetuspto-grants-1992_09
ORD IDord-ce1f23167bbc4e8281abd639a6e1f6cb
Source noteuspto-grants-1992_09