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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604840Generated: October 26, 2026

Chlorodimethylaluminum → (R)-1-Chloro-6-trimethylsilanyl-hex-4-yn-2-ol

https://huagongshe.com/reaction/1604840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodimethylaluminumHCID 79147—
ReactantTrimethyl-2-propynylsilaneHCID 83378—
Reactant(-)-EpichlorohydrinHCID 2734062—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
Product(R)-1-Chloro-6-trimethylsilanyl-hex-4-yn-2-olHCID 2131006466.6%

Reaction Steps

14.11 g (126 mmol) of propargyltrimethylsilane was dissolved in 125 ml of abs. toluene and cooled to -17°. 81.1 ml of nBuLi (1.55 M, hexane) was slowly added while keeping the temperature below -5°. 5 Minutes later, 126 ml of Me2AlCl (1 M, hexane) was added to this solution of the Li-acetylide. The temperature was then lowered to -45° and 6.90 ml of (R)-epichlorohydrine (88 mmol), dissolved in 50 ml of toluene, was added. The cooling bath was then removed and the reaction mixture allowed to reach ambient temperature during 24h. After careful quenching with icecold water and filtration, the product was extracted with ether, washed with NH4Cl, dried over sodium sulfate and the solvents removed i. V. Flash chromatography (SiO2, hexane/AcOEt=86/14) yielded 12.01 g of (R)-1-chloro-6-trimethylsilanyl-hex-4-yn-2-ol as colorless oil, 97% pure according to GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994569
Source datasetuspto-grants-1999_11
ORD IDord-b676aca0d32548d08e433deab0417857
Source noteuspto-grants-1999_11