HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057142Generated: November 1, 2026
Chlorotrimethylsilane → (6-Chlorohex-1-yn-1-yl)trimethylsilane
https://huagongshe.com/reaction/1057142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 6-Chloro-1-hexyne | HCID 272001 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (6-Chlorohex-1-yn-1-yl)trimethylsilane | HCID 13839479 | 93% |
Reaction Steps
To a solution of 6-chlorohex-1-yne (100 mL, 94.6 g, 0.82 mol) in anhydrous Et2O (500 mL) at −78° C., n-butyllithium (2.5 M in hexane, 360 mL, 0.90 mol) was added over 40 minutes. The resulting mixture was stirred for 30 minutes at −78° C. Chlorotrimethylsilane (125 mL, 1.0 mol) was then added. The mixture was allowed to warm to room temperature and stirred for 16 h. The reaction mixture was carefully quenched with saturated aqueous NH4Cl (300 mL) at room temperature and extracted with Et2O (2×200 mL). The combined organic layers were washed with brine (200 mL), dried over anhydrous Na2SO4, and concentrated in vacuo to afford the title compound (144 g, yield 93%). 1H NMR (DMSO-d6, 400 MHz): δ 3.65 (t, 2H), 2.25 (t, 2H), 1.82-1.75 (m, 2H), 1.58-1.51 (m, 2H), 0.12 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09399646B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-c70bb246a41d44b49bfa8430f152839f |
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| Source note | uspto-grants-2016_07 |
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