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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant6-Chloro-1-hexyneHCID 272001—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(6-Chlorohex-1-yn-1-yl)trimethylsilaneHCID 1383947993%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399646B2
Source datasetuspto-grants-2016_07
ORD IDord-c70bb246a41d44b49bfa8430f152839f
Source noteuspto-grants-2016_07