HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → Methyl 5-(3-chloropropoxy)-4-methoxy-2-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Methyl 3-(3-chloropropoxy)-4-methoxybenzoate | HCID 11623039 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-(3-chloropropoxy)-4-methoxy-2-nitrobenzoate | HCID 11666631 | 61% |
Reaction Steps
The aforementioned J. Med. Chem., 44, 3965 (2001) further describes a process for preparing a 4-alkoxy-5-halogenoalkoxy-2-nitrobenzoic acid compound from a 4-alkoxy-3-hydroxybenzoic acid compound. For example, methyl 3-hydroxy-4-methoxybenzoate is reacted with 3-chloropropyl p-toluenesulfonate in an aqueous potassium carbonate solution in the presence of tricaprylmethyl ammonium chloride to produce methyl 3-(3-chloropropoxy)-4-methoxybenzoate, and the methyl 3-(3-chloropropoxy)-4-methoxybenzoate is reacted with 70% nitric acid in a mixture of dichloromethane and acetic acid, to give methyl 5-(3-chloropropoxy)-4-methoxy-2-nitrobenzoate in 61% yield (based on the amount of methyl 3-hydroxy-4-methoxybenzoate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367824B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-4b5963af7db3486097dc577675640531 |
| Source note | uspto-grants-2013_02 |