HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoaniline → HCID 22225739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | (But-3-yn-1-yloxy)(tert-butyl)dimethylsilane | HCID 4304567 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Butylamine | HCID 8007 | — |
| Product | HCID 22225739 | HCID 22225739 | — |
Reaction Steps
A mixture of 1-(t-butyldimethylsilyloxy)-3-butyne (10 mmol) and m-bromoaniline (10 mmol) in n-butylamine (50 mL) under a nitrogen atmosphere is treated with tetrakis(triphenylphosphine)palladium (0) (0.17 g) and then heated to reflux for 18 hr. After removing the solvent in vacuo, the residue is dissolved in CH2Cl2 and washed with saturated NaHCO3. The combined organic solution is dried over magnesium sulfate, filtered and evaporated to give the above described silyl protected adduct.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06130234 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-2bffa424f5384ed486a6d8f0e064a4a9 |
| Source note | uspto-grants-2000_10 |