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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581616Generated: October 25, 2026

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

https://huagongshe.com/reaction/581616

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 (1.55M, hexane) was slowly added while keeping the temperature below -5°. 5 Minutes later, 126 ml of Me2AlCl (1M, 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 24 h. 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 numberUS05919986
Source datasetuspto-grants-1999_07
ORD IDord-8c2604e7c6b74d7d8b0146df22061afa
Source noteuspto-grants-1999_07