HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylboronic Acid → HCID 67214827, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 795837 | HCID 795837 | — |
| Product | HCID 67214827 | HCID 67214827 | — |
Reaction Steps
Using Preparation Method 2, N-(3-pyridylmethyl)-3-bromobenzamide was reacted with phenylboronic acid. The resulting reaction mixture was purified using SiO2 with CH2Cl2/MeOH 98:2 to 90:10. A colourless oil was obtained (87%). NMR 1H (ppm, CDCl3): 8.87 (s, 1H), 8.73 (d, J4=4.5 Hz, 1H), 8.28 (t, J4=2.0 Hz, 1H), 8.03-7.94 (m, 3H), 7.89 (d, J3=6.9 Hz, 2H), 7.75-7.50 (m, 5H), 6.17 (br. t., 1H), 4.91 (d, J3=5.9 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07956216B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-308c83b7c21141ab9d140248caf1d2a1 |
| Source note | uspto-grants-2011_06 |