Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244114Generated: November 2, 2026

Trimethylsilylacetylene → 6-Trimethylsilanylethynylbenzothiazol

https://huagongshe.com/reaction/2244114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant6-Bromo-1,3-benzothiazoleHCID 2795171—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTriethylamineHCID 8471—
Product6-TrimethylsilanylethynylbenzothiazolHCID 23154582—

Reaction Conditions

Temperature80 °C

Reaction Steps

Trimethylsilylacetylene (106 ml), copper (I) iodide (0.948 g), and bis(triphenylphosphine) palladium(II) dichloride (1.75 g) were added to 6-bromobenzothiazole (53.3 g) in triethylamine (260 ml), and the mixture was stirred for 2.5 hours at 80° C. After the solvent was evaporated, the resultant residue was loaded on a short column (silica gel; hexane:ethyl acetate=2:1) for elution. The residue from the eluate was recrystallized from a mixed solvent of hexane-ethyl acetate, and consequently, 6-trimethylsilanylethynylbenzothiazole (20.0 g) was obtained as a colorless powder (mp: 104.5-105.0° C.). By repeated subjecting the filtrate to recrystallization repeated (n-hexhane-ethyl acetate), secondary crystals (12.1 g), tertiary crystals (9.68 g), and quaternary crystals (4.61 g) were obtained as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678810B2
Source datasetuspto-grants-2010_03
ORD IDord-2a31c4b0eacf465781270bd3d2a75f73
Source noteuspto-grants-2010_03