HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610916Generated: October 25, 2026
Cyclohexane → 2-Chloro-N,N-diethyl-6-(trimethylgermyl)benzamide
https://huagongshe.com/reaction/610916
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Chlorotrimethylgermane | HCID 73723 | — |
| Reactant | 2-Chloro-N,N-diethylbenzamide | HCID 82566 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-N,N-diethyl-6-(trimethylgermyl)benzamide | HCID 18630044 | 45% |
Reaction Steps
A solution of 1.3M s-BuLi in cyclohexane (21.8 mL, 28.3 mmol) was added dropwise to a dry ice/acetone cooled solution of the compound of example e (4.6 g, 21.7 mmol) in THF (60 mL), maintaining the internal reaction temperature ≤-65° C. This mixture was stirred at -78° C. for 45 min, then was quenched by the dropwise addition of a solution of trimethylchlorogermane (5.0 g, 32.6 mmol) in THF (30 mL), again maintaining the internal reaction temperature ≤-65° C. The reaction was warmed to 0° C., diluted with ether, and extracted with 10% HCl (2×) followed with sat aq NaHCO3. The ether was dried (MgSO4), concentrated, and purified by HPLC with 6% EtOAc in hexanes to afford 3.2 g of the title compound as a white solid, a 45% yield. m.p. 47-48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998466 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-7884cfec0318498f853407cf1320d2d9 |
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| Source note | uspto-grants-1999_12 |
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