HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 57419866, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-Hydroxy-5-(methanesulfonyl)benzaldehyde | HCID 57419865 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57419866 | HCID 57419866 | — |
Reaction Steps
2-Hydroxy-5-methanesulfonyl-benzaldehyde (0.200 g, 1.0 mmol), ethylamine (2M in THF; 0.75 mL, 1.5 mmol), and sodium cyanoborohydride (0.095 g, 1.5 mmol) were combined in MeOH (10 mL). 4Å Molecular sieves were added, followed by acetic acid (0.09 mL, 1.5 mmol), and the reaction was stirred for 1 hour. The mixture was filtered, and H2O (0.5 mL) was added and the solution was concentrated. The residue was partitioned between EtOAc (100 mL) and brine (20 mL), and the mixture was neutralized with 1N aqueous HCl (1 mL) and extracted six times with EtOAc, until minimal product was seen in the aqueous layer by analytical tlc. The combined organic layers were dried, filtered, and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338484B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-d2547d5ae0d14eee8f06d149f641d163 |
| Source note | uspto-grants-2012_12 |