HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768045Generated: October 30, 2026
Potassium Carbonate → [4-(4-[1,2,3]Triazol-1-yl-but-1-enyl)-phenyl]-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/1768045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | tert-butyl N-(4-iodophenyl)carbamate | HCID 2773612 | — |
| Reactant | 1-But-3-ynyl-1H-[1,2,3]triazole | HCID 18453522 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [4-(4-[1,2,3]Triazol-1-yl-but-1-enyl)-phenyl]-carbamic acid tert-butyl ester | HCID 69490216 | 33% |
Reaction Steps
A solution of 1-but-3-ynyl-1H-[1,2,3]triazole (0.76 g, 6.3 mmol) in anhydrous THF (50 ml) is treated with 9-BBN (0.5 M in THF, 27.6 ml, 13.8 mmol) at 0° C. and stirred for 2 h. This mixture is added to a solution of (4-iodo-phenyl)-carbamic acid tert-butyl ester (2 g, 6.3 mmol), [Pd(PPh3)2]Cl2 (0.51 g, 0.63 mmol) and aqueous potassium carbonate (3M, 6.3 ml, 18.8 mmol) in N,N-dimethyl formamide (50 ml) and stirred for 2 h at 70° C. After cooling to room temperature ethyl acetate (100 ml) is added and the solution extracted with water (2×50 ml). The organic layer is concentrated and the crude product purified by flash column chromatography (ethyl acetate/heptane 3:1) and washing with diethyl ether to yield [4-(4-[1,2,3]triazol-1-yl-but-1-enyl)-phenyl]-carbamic acid tert-butyl ester as beige solid (0.65 g, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07235574B2 |
|---|
| Source dataset | uspto-grants-2007_06 |
|---|
| ORD ID | ord-4a5517bbb3114879b0b2ce36d7c3711b |
|---|
| Source note | uspto-grants-2007_06 |
|---|