HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452354Generated: October 27, 2026
Germane, chlorotris(1-methylethyl)- → 2-(3,5-Dimethylphenyl)-6-(triisopropylgermyl)quinoline
https://huagongshe.com/reaction/452354
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Germane, chlorotris(1-methylethyl)- | HCID 606958 | — |
| Reactant | 6-Bromo-2-(3,5-dimethylphenyl)quinoline | HCID 68193681 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3,5-Dimethylphenyl)-6-(triisopropylgermyl)quinoline | HCID 86669969 | 82.7% |
Reaction Steps
6-Bromo-2-(3,5-dimethylphenyl)quinoline (5.3 g, 16.98 mmol) and 150 mL anhydrous THF were added in a dry two-necked round bottom flask and cooled down to −78° C. 7.2 mL BuLi (2.5 M) was added dropwise. The solution was stirred for 45 minutes and 4.4 mL (20.37 mmol) of chlorotriisopropylgermane was slowly added with a syringe. The solution was stirred for 4 h and monitored by GC until the reaction was finished. The reaction mixture was purified by column and distillation. ˜6.1 g colorless liquid was obtained after distillation. GC-MS confirmed the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492006B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-b48769045e0440e1bb5d5aaa82ab2620 |
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| Source note | uspto-grants-2013_07 |
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