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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-3-methoxypropaneHCID 524551—
ReactantMethyl 2-amino-3-nitrobenzoateHCID 607264—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(3-methoxypropylamino)-3-nitrobenzoateHCID 5819882178.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138168B1
Source datasetuspto-grants-2012_03
ORD IDord-d610d45c937d4f05a1fdc7a8ad1fe604
Source noteuspto-grants-2012_03