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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593397Generated: October 30, 2026

Hydrochloric Acid → (S)-tert-Butyldimethyl(oct-1-yn-3-yloxy)silane

https://huagongshe.com/reaction/593397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1-Octyn-3-ol, (3S)-HCID 2734534—
SolventDichloromethaneHCID 6344—
Product(S)-tert-Butyldimethyl(oct-1-yn-3-yloxy)silaneHCID 10752577—

Reaction Steps

The procedure of Noyori (Suzuki, M., et al., J. Med. Chem. 41, 3084-3090 (1998)) was used. Imidazole (971 mg, 14.3 mmol) and t-butylchlorodimethylsilane (1.43 g, 9.51 mmol) were added to a solution of (S)-1-octyn-3-ol SI-8 (1.00 g, 1.16 ml, 7.92 mmol) in CH2Cl2 (18 ml), cooled to 0° C. The reaction mixture was then stirred at room temperature for 24 h before being poured into 1 M HCl (50 ml). The mixture was extracted with 40/60 petroleum ether (3×50 ml). The combined organic phases were washed with brine (50 ml) before being dried (MgSO4), filtered, and concentrated to give the title compound SI-7 (1.89 g, 99%) as a clear, colourless oil. Analytical data consistent with the literature (Nicolaou, K. C. et al., A. J. Am. Chem. Soc. 107, 7515-7518 (1985); Cmrecki, V. et al., Tetrahedron 66, 6550-6564 (2010)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242954B2
Source datasetuspto-grants-2016_01
ORD IDord-ef0b8077dbd04974970447d63ba127c7
Source noteuspto-grants-2016_01