HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycolaldehyde dimer → Ethyl 2-[4-(2-hydroxyethylamino)phenyl]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycolaldehyde dimer | HCID 186078 | — |
| Reactant | Methyl 2-(4-aminophenyl)propionate | HCID 3016109 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 2-[4-(2-hydroxyethylamino)phenyl]propionate | HCID 22118659 | — |
Reaction Steps
Following the procedure of Himmelsbach, et. al., EP 0587134, Example V, glycolaldehyde dimer (Aldrich) (1 mmol) is added to a solution of methyl 2-(4-aminophenyl)propionate (1 mmol) in aqueous CH3CN (pH 6-7) (10 mL), followed by NaBH3CN (1.2 mmol), and the mixture is allowed to stir for 1 h. The mixture concentrated to an oil, and the residue is dissolved in a mixture of ice water and EtOAc. The aqueous layer is neutralized with 4N NaOH and washed with EtOAc. The organic phase is concentrated to an oil. A solution of the oil in EtOAc is chromatographed (silica gel, gradient, 5-30% CH3OH/CH2Cl2 -0.1% HOAc). The fractions containing the product are combined and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06159964 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-2440400fb1b84b7294d50909f6adc886 |
| Source note | uspto-grants-2000_12 |