Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 4-Bromo-2,1,3-benzothiadiazole | HCID 736492 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68407726 | HCID 68407726 | — |
Reaction Steps
4-Bromobenzo[c][1,2,5]thiadiazole (0.378 g, 1.76×10−3 mol), Pd(PPh3)4 (0.125 g, 1.68×10−4 mol), CuI (0.014 g, 7.4×10−5 mol), THF (20 ml), diisopropylamine (1.00 ml), and (trimethylsilyl)acetylene (1.00 ml, 7.1×10−3 mol) were added to a 50-ml Schlenk tube. N2 was bubbled through the mixture for 5 min, following which the reaction was stirred at 45° C. for 20 h. After cooling, the solvent was evaporated and the residue was chromatographed on silica gel using 1:1 hexanes:CHCl3 as the eluent. Yield=0.398 g (97.3% based on 0.378 g of 4-bromobenzothiadiazole). 1H NMR (500 MHz, CDCl3): δ 7.88 (m, 1H, Ph-H), 7.67 (m, 1H, Ph-H), 7.45 (m, 1H, Ph-H), 0.33 (s, 9H, —Si—CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842758B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-b37173ab8ff64aa1ad8a04878c7c4f9b |
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| Source note | uspto-grants-2010_11 |
|---|