Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494664Generated: October 30, 2026

Water → (6-Chlorohex-1-yn-1-yl)trimethylsilane

https://huagongshe.com/reaction/1494664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant1-Chloro-4-iodobutaneHCID 82527—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(6-Chlorohex-1-yn-1-yl)trimethylsilaneHCID 13839479—

Reaction Steps

A solution of trimethylsilylacetylene (4.9 g., Aldrich) in dry tetrahydrofuran (40 ml.) was stirred at 0° under a current of nitrogen and n-butyllithium (31.25 ml. of 1.6M solution in hexane) was added dropwise. The solution was stirred for 30 minutes and a solution of 1-chloro-4-iodobutane (10.9 g.) in dry tetrahydrofuran (30 ml.) was added. The reaction mixture was allowed to warm to 20° and stirred for 18 hours. The mixture was poured into water and the aqueous mixture was extracted with diethyl ether. The ethereal extracts were washed with water and dried over anhydrous magnesium sulphate. The solvent was removed in vacuo. 6-Chloro-1-trimethylsilylhex-1-yne was obtained as a yellow liquid and was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026874
Source datasetuspto-grants-1991_06
ORD IDord-e3dfe52249bc4c5499376507bc2e3b7b
Source noteuspto-grants-1991_06