HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 69265671, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl 3-aminophenylacetate | HCID 13054266 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Product | HCID 69265671 | HCID 69265671 | — |
| Product | HCID 86719104 | HCID 86719104 | — |
Reaction Steps
To the solution of methyl 2-(3-aminophenyl)acetate (150 mg, 0.83 mmol) and acetaldehyde (80.5 mg, 1.83 mmol) in methanol (6 mL) was added NaBH3CN (130.3 mg, 2.08 mmol) and AcOH (1 drop, cat.). The mixture was stirred at room temperature for 12 h. Then, the reaction was quenched with aqueous ammonium chloride and extracted with DCM. The organic layer was with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by a standard method to get methyl 2-(3-(diethylamino)phenyl)acetate and methyl 2-(3-(ethylamino)phenyl)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029531B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-65808d2b51f64db3885a8b7ee8f3af34 |
| Source note | uspto-grants-2015_05 |