HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716588Generated: October 25, 2026
Magnesium → 2-(Triethoxygermyl)-thianthrene
https://huagongshe.com/reaction/716588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Bromothianthrene | HCID 13213122 | — |
| Reactant | Germanium(IV) ethoxide | HCID 16684444 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Triethoxygermyl)-thianthrene | HCID 89287683 | 30.5% |
Reaction Steps
A 3-neck 500 mL flask was filled with magnesium turnings (8 g), THF (100 g) and tetraethoxygermane (35 g), and heated to reflux. Crude 2-bromothianthrene (30 g) from Example 1 was added to the flask in small portions. Grignard started after a few minutes and kept refluxing by its own heat for ten minutes. The reaction was allowed to cool for 1 hour, after which magnesium salts were precipitated with heptanes (300 mL). The solution was filtered, followed by evaporation of volatiles by rotary evaporator. The material was distilled three times at <1 mbar, giving colorless 2-(triethoxygermyl)-thianthrene (bp. 180 . . . 210° C., 11 g, 30.5% overall yield based on 2-bromothianthrene, purity 99.5% by GC/MS). FIG. 8 shows the mass spectrum of the compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09190616B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-863df8351ebf4d05ae633fa67c06e385 |
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| Source note | uspto-grants-2015_11 |
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