HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinone → methyl 5-hydroxy-2-(methoxymethyl)-1-methylindole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinone | HCID 4650 | — |
| Reactant | HCID 85255412 | HCID 85255412 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | methyl 5-hydroxy-2-(methoxymethyl)-1-methylindole-3-carboxylate | HCID 10198835 | 22% |
Reaction Steps
3.1 g of 1,4-benzoquinone (28.7 mmol) was dissolved in 50 ml of acetic acid to which was subsequently added dropwise 2.28 g (14.3 mmol) of methyl 4-methoxy-3-methylamino-2-butenoate and the mixture was stirred for 5 hours at room temperature. After the solvent was distilled off under reduced pressure, the resulting residue was dissolved in ethyl acetate, washed with water and saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. After anhydrous magnesium sulfate was filtered off and the solvent was distilled off under reduced pressure, the residue was purified by a silica gel column chromatography (eluent: hexane-ethyl acetate, 2:1) to obtain 0.78 g of the title compound with a yield of 22%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05344938 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-3523da35b3784fbbb29d60e458d8d907 |
| Source note | uspto-grants-1994_09 |