HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Dimethyl (4-methoxy-2-nitrobenzyl)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Dimethyl (4-methoxy-2-nitrophenyl)methylidenemalonate | HCID 54325413 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Dimethyl (4-methoxy-2-nitrobenzyl)malonate | HCID 53955072 | 75.5% |
Reaction Steps
Sodium borohydride (3.36 g) was added to a methanol (200 ml) solution of dimethyl (4-methoxy-2-nitrophenyl)methylidenemalonate (25 g) under ice-cooling. The reaction mixture was stirred at room temperature for one hour and then neutralized by adding dropwise 1N aqueous hydrochloric acid solution. The reaction mixture was concentrated and extracted with ethyl acetate. The organic layer was washed with water, a saturated aqueous potassium bicarbonate solution and a saturated aqueous sodium chloride solution, then dried and concentrated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/4) to obtain the entitled compound (19 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329389B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-8acfaa4e04714efea2c6522adb54d879 |
| Source note | uspto-grants-2001_12 |