HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354143Generated: November 3, 2026
2-Methyl-3-butyn-2-ol → HCID 25023309, compound
https://huagongshe.com/reaction/2354143
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyl-3-butyn-2-ol | HCID 8258 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-(2-bromo-4-fluorophenyl)acetamide | HCID 688184 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Product | HCID 25023309 | HCID 25023309 | — |
Reaction Steps
0.32 g (1.2 mmol, purity 99%) triphenylphosphine, 0.085 g (0.12 mmol, purity 99%) bis-triphenylphosphine palladium dichloride, and 0.14 g (0.72 mmol, purity 98%) copper(I)iodide are added to a mixture of 56.8 g (0.24 mol, purity 98%) N-(2-bromo-4-fluorophenyl)acetamide, 30.9 g (0.264 mol, purity 98%) 2-methylbut-3-yn-2-ol and 121.4 g (1.2 mol) triethylamine and the mixture is heated for 6 hours while stirring at 85° C. The surplus triethylamine is distilled off in a vacuum, approximately 170 ml toluene is added, the same quantity of water is added, and the phases are separated at ˜70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07750186B2 |
|---|
| Source dataset | uspto-grants-2010_07 |
|---|
| ORD ID | ord-d60cc8e16f0f429a822ea7d2673482bc |
|---|
| Source note | uspto-grants-2010_07 |
|---|