HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853805Generated: October 31, 2026
Sodium Bicarbonate → HCID 10869392, compound
https://huagongshe.com/reaction/853805
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Cyanophenylboronic acid | HCID 2734326 | — |
| Reactant | HCID 10911902 | HCID 10911902 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10869392 | HCID 10869392 | 64% |
Reaction Steps
Continuing with Scheme 3, to a stirred solution of 15 (1.245 g, 5 mmol), and tetrakis(triphenylphosphine) palladium (288 mg) in toluene (15 mL) under a nitrogen atmosphere was added 10 mL of a 1 M aqueous solution of NaHCO3 followed by 4-cyanophenyl boronic acid (821 mg, 4.6 mmol) in 5 mL of methanol. The vigorously stirred mixture was warmed to 80° C. for 24 h, then cooled, and the precipitate was filtered. The precipitate was partitioned between methylene chloride (300 mL) and 1 M aqueous NaHCO3 (50 mL). The organic layer was dried (Na2SO4), and then concentrated to dryness under reduced pressure to afford 16 in 64% yield; mp 276–277° C. (DMF). 1H nmr(DMSO-d6); δ 7.49 (d, J=3.6 Hz, 1H), 7.59 (d, J=3.6 Hz, 1H), 7.95 (d, J=8.7 Hz, 2H), 8.10 (d, J=8.7 Hz, 2H). 8.14 (d, J=8.1 Hz 1H), 8.49 (dd, J=8.1, 1.5 Hz, 1H), 9.29 (d, J=1.5 Hz, 1H). 13C nmr; δ 153.0, 149.7, 146.3, 133.1, 132.8, 131.4, 130.4, 129.0, 128.5, 124.4, 118.6, 117.4, 113.2, 111.8, 110.0. Calcd. for C17H9N3O: C, 75.26; H, 3.34; N, 15.49. Found. C, 75.02; H, 3.35; N, 15.39.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07256203B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-682ff579a222460e9eff70cd7cd42612 |
|---|
| Source note | uspto-grants-2007_08 |
|---|