HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244304Generated: October 25, 2026
Triethoxychlorosilane → Silane, triethoxyethynyl-
https://huagongshe.com/reaction/244304
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethoxychlorosilane | HCID 78398 | — |
| Reactant | HCID 178418486 | HCID 178418486 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Silane, triethoxyethynyl- | HCID 79778 | 80% |
Reaction Steps
Chlorotriethoxysilane (2.0 mL, 10 mmol, 1.0 equiv) was added to a stirred solution of 0.5M ethynylmagnesium bromide (20 mL, 10 mmol, 1.0 equiv) in tetrahydrofuran (10 mL) at −78° C. The resulting heterogeneous light brown mixture was immediately warmed to 23° C. and stirred for 1 h. The resulting homogeneous light brown solution was heated to 50° C. and stirred for 4 h. The cooled reaction mixture was concentrated under vacuum. The resulting tan powder was slurried in hexane (50 mL), vacuum filtered, and rinsed with additional hexane (3×25 mL). The filtrates were dried over magnesium sulfate, gravity filtered, and concentrated under vacuum to provide the title compound as a pale yellow oil (1.5 g, 80% yield): IR (thin film) 3252 (w), 2976 (s), 2929 (m), 2913 (w), 2890 (m), 2046 (m) cm−1; 1H NMR (400 MHz, CDCl3) δ 3.90 (q, J=7 Hz, 6H), 2.35 (s, 1H), 1.23 (t, J=7 Hz, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658568B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-478d6e4e44144b7fa5cf2ef8b91e555a |
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| Source note | uspto-grants-2014_02 |
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