HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244114Generated: November 2, 2026
Trimethylsilylacetylene → 6-Trimethylsilanylethynylbenzothiazol
https://huagongshe.com/reaction/2244114
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 6-Bromo-1,3-benzothiazole | HCID 2795171 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-Trimethylsilanylethynylbenzothiazol | HCID 23154582 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678810B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-2a31c4b0eacf465781270bd3d2a75f73 |
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| Source note | uspto-grants-2010_03 |
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