HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthaleneboronic acid → HCID 86720518, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthaleneboronic acid | HCID 254532 | — |
| Reactant | 6-Bromo-3-pyridinecarboxaldehyde | HCID 11769234 | — |
| Product | HCID 86720518 | HCID 86720518 | — |
Reaction Steps
Synthesized using compound 43c (720 mg, 3.87 mmol) and 1-naphthaleneboronic acid (1.00 g, 5.81 mmol) according to Method C. Crude product was purified by flash chromatography on silica-gel using a mixture of hexane/ethyl acetate (8:1) as eluent. Orange solid. Yield: 733 mg, 81%. 1H NMR (CDCl3, 500 MHz): δH (ppm)=7.50-7.62 (m, 3H), 7.65-7.69 (m, 1H), 7.77-7.81 (m, 1H), 7.92-8.00 (m, 2H), 8.10-8.14 (m, 1H), 8.31 (dd, J=7.9, 2.2 Hz, 1H), 9.25 (dd, J=2.2, 0.9 Hz, 1H), 10.22 (s, 1H); 13C NMR (CDCl3, 125 MHz): δC (ppm)=125.1, 125.2, 125.4, 126.2, 127.0, 128.0, 128.5, 129.7, 130.0, 130.7, 134.0, 136.1, 137.2, 152.1, 164.6, 190.5; MS (ESI): m/z=234.29 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09394290B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-1d91bb45b3884f02975479e226baa5cb |
| Source note | uspto-grants-2016_07 |