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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromo-2,6-diisopropylaniline | HCID 11780114 | — |
| Reactant | Chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilane | HCID 58526148 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58526155 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173828B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-4bcb3e5cc2a541c98d0859388db2b6fb |
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| Source note | uspto-grants-2012_05 |
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