HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boronic Acid → 2-(3-Thienyl)-3-pyridinecarboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | Thiophene-3-boronic acid | HCID 581760 | — |
| Reactant | 2-Bromonicotinaldehyde | HCID 4714951 | — |
| Product | 2-(3-Thienyl)-3-pyridinecarboxaldehyde | HCID 2764564 | — |
Reaction Steps
2-(thiophen-3-yl)nicotinaldehyde was prepared using the general boronic acid coupling procedure for 2-bromonicotinaldehyde and thiophen-3-ylboronic acid (60 mg, 101.8 mg theoretical, 58.9%). LC-MS m/z 190.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901145B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-6cc2de8e7a2244b68eaf556dacea9461 |
| Source note | uspto-grants-2014_12 |