HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504246Generated: October 30, 2026
HCID 21259639, compound → HCID 123309382, compound
https://huagongshe.com/reaction/1504246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21259639 | HCID 21259639 | — |
| Reactant | HCID 178443577 | HCID 178443577 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 123309382 | HCID 123309382 | 49% |
Reaction Steps
Trichloro(2-ethylhexyl)silane (synthesized in accordance with J. Am. Chem. Soc. 2008, 130, 16144-16145, 24.8 g) was placed in a 300 mL four-necked flask in a nitrogen atmosphere, and dissolved in tetrahydrofuran (100 mL). The resulting solution was cooled to 0° C., and a solution of n-octyl magnesium bromide in diethyl ether (Sigma-Aldrich Co. LLC., 2.00 M, 50.0 mL) was added dropwise. The reaction solution was agitated for about 30 minutes at 7° C., and then agitated for about 3 hours at room temperature. The solvent was then distilled off with an evaporator. Hexane was added to the resulting crude product, which was then filtered, after which the solvent was again distilled off. Finally, distillation purification (111° C., 0.61 torr) was performed to obtain the target dichloro(2-ethylhexyl)n-octylsilane (Compound G6, 15.9 g, yield 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212254B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-fdfb03509d2341ea84c948588f776f42 |
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| Source note | uspto-grants-2015_12 |
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