HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → N-Methyl-4-[(trimethylsilyl)ethynyl]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Benzenamine, 4-bromo-N-methyl- | HCID 2757052 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | N-Methyl-4-[(trimethylsilyl)ethynyl]aniline | HCID 123875059 | 37% |
Reaction Steps
To a suspension of 4-bromo-N-methylaniline (500 mg, 2.7 mmol), trimethylsilyl acetylene (527 mg, 5.4 mmol), CuI (92 mg, 0.5 mmol) and PPh3 (233 mg, 0.9 mmol) in TEA (20 mL) was added PdCl2(PPh3)2 (94 mg, 0.1 mmol) at r.t. under N2. The reaction was stirred at reflux overnight. The reaction was filtered, concentrated, and purified by silica gel chromatography (PE:EtOAc=20:1) to give 200 mg (37%) of the title compound as a yellow oil. [M+H] Calc'd for C12H17NSi, 204. Found, 204.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447046B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-9b3f502c99cf41978d1aead30105a627 |
| Source note | uspto-grants-2016_09 |