HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096635Generated: November 3, 2026
Sodium Iodide → Methyl 2-(3-methoxypropylamino)-3-nitrobenzoate
https://huagongshe.com/reaction/1096635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-3-methoxypropane | HCID 524551 | — |
| Reactant | Methyl 2-amino-3-nitrobenzoate | HCID 607264 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(3-methoxypropylamino)-3-nitrobenzoate | HCID 58198821 | 78.1% |
Reaction Steps
Methyl 2-amino-3-nitrobenzoate (3.82 mmol, 0.75 g) in DMF (20 mL) was added NaI (8.40 mmol, 1.26 g). The reaction solution was stirred at 0° C. for 5 min and then added NaH (5.00 mmol, 0.20 g) at 0° C. The reaction solution was stirred at 0° C. for 30 min and then added 1-bromo-3-methoxypropane (5.00 mmol, 0.77 g). The reaction solution was heated to 80° C. and kept stirring at 80° C. for 6 hr. After cooling down the reaction solution was poured into H2O, extracted with EtOAc. The extract was washed with H2O, brine dried over MgSO4 and filtered. The filtrate was concentrated in vacuo and purified by flash chromatography (silica gel, EtOAc-hexane: 5:95) to afford methyl 2-(3-methoxypropylamino)-3-nitrobenzoate (44A) (1.49 mmol, 800 mg, yield: 78.1%). ESI-MS: m/z 269.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08138168B1 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-d610d45c937d4f05a1fdc7a8ad1fe604 |
|---|
| Source note | uspto-grants-2012_03 |
|---|