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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922328Generated: November 1, 2026

4-Bromo-2,6-diisopropylaniline → HCID 58526155, compound

https://huagongshe.com/reaction/1922328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2,6-diisopropylanilineHCID 11780114—
ReactantChloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilaneHCID 58526148—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58526155HCID 58526155—

Reaction Steps

Under an argon atmosphere, to a solution of 18.9 g (73.8 mmol) of 4-bromo-2,6-diisopropylaniline in 200 ml of THF, 29.5 ml of 2.5 M (73.8 mmol) nBuLi in hexanes was added at −80° C. This mixture was warmed for ca. 1 hour to ambient temperature. Then, the resulting solution was added dropwise over ca. 1 hour, while vigorously stirring, to a solution of 17.9 g (73.8 mmol) of chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilane in 100 ml of THF. The resulting mixture was stirred overnight at ambient temperature, and then, evaporated to dryness. To the residue, 150 ml of toluene was added. This mixture was filtered through a glass frit (G4). The filtrate was evaporated to dryness. Fractional distillation gave a yellow liquid, bp 180° C./0.1 mm Hg. The product crystallizes slowly at ambient temperature. Yield 11.9 g (35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173828B2
Source datasetuspto-grants-2012_05
ORD IDord-4bcb3e5cc2a541c98d0859388db2b6fb
Source noteuspto-grants-2012_05