HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Carboxybenzaldehyde → HCID 9980457, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Carboxybenzaldehyde | HCID 12077 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68869657 | HCID 68869657 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 9980457 | HCID 9980457 | 31% |
Reaction Steps
N-(3-aminobenzyl)-1,1′-biphenyl-4-carboxamide (20 mg, 0.07 mmol) was dissolved in acetic acid (0.5 ml). 3-Carboxybenzaldehyde (14 mg, 0.09 mmol) was added and then sodium borohydride (11 mg, 0.28 mmol) was added. The mixture was stirred at room temperature for 2 hours and evaporated to dryness. DCM was added into the residue. The mixture was loaded on a column (ISOLUTE® SI, 500 mg/3 ml). It was eluted with DCM, MeOH/DCM (0.5:99.5) and then MeOH/DCM (1:99). The product fractions were combined and the solvent was removed, Re-chromatography of the residue on a column (ISOLUTE® SI, 1 g/6 ml) using DCM, MeOH/DCM (0.5:99.5) and then MeOH/DCM (1:99) as eluant gave 9 mg the desired product, yield 31%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07521461B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-6c709838121041e289db0d495d180ef1 |
| Source note | uspto-grants-2009_04 |