HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-(acetoxymethyl)-4-nitrobenzoate → Methyl 3-(hydroxymethyl)-4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-(acetoxymethyl)-4-nitrobenzoate | HCID 18371998 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-(hydroxymethyl)-4-nitrobenzoate | HCID 18372008 | — |
Reaction Steps
In a 5-liter three-necked round-bottomed flask equipped with a reflux condenser, overhead stirrer and nitrogen inlet, was placed 318 g of the previously prepared methyl 3-acetoxymethyl-4-nitrobenzoate and 3.2 l of anhydrous methanol. To the resulting solution was bubbled in 40 g of hydrogen chloride and the resulting mixture was refluxed for 3 hours. After cooling to room temperature the solvent was removed using a rotary evaporator yielding 273 g of methyl 3-hydroxymethyl-4-nitrobenzoate as a yellow solid containing traces of methanol, which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05929098 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-ef0ee0219eae46338661525933d0dc48 |
| Source note | uspto-grants-1999_07 |