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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275063Generated: November 3, 2026

Methyl iodide → N-t-butoxycarbonyl-N-methyl-5-methoxy-2-nitroaniline

https://huagongshe.com/reaction/1275063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl (5-methoxy-2-nitrophenyl)carbamateHCID 10199249—
SolventDimethylformamideHCID 6228—
ProductN-t-butoxycarbonyl-N-methyl-5-methoxy-2-nitroanilineHCID 15544600—

Reaction Steps

A solution of 49.6 g of N-t-butoxycarbonyl-5-methoxy-2-nitroaniline [prepared as described in step (b) above] in 300 ml of dehydrated dimethylformamide was added, whilst ice-cooling, to a suspension of 12.0 g of sodium hydride (as a 55% w/w dispersion in mineral oil) in 300 ml of dehydrated dimethylformamide, and the resulting mixture was stirred at room temperature for 30 minutes, after which 17.2 ml of methyl iodide were added at room temperature. The reaction mixture was stirred for 1 hour, after which it was allowed to stand overnight at room temperature. It was then concentrated to about one-fifth of its original volume by evaporation under reduced pressure. The concentrate was mixed with ice-water and the resulting aqueous mixture was extracted with ethyl acetate. The extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous sodium sulfate. On distilling off the solvent, there were obtained 52.1 g of the title compound, melting at 122-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159997
Source datasetuspto-grants-2000_12
ORD IDord-1df1b8dc87ff487e8fb35e038c5c4ced
Source noteuspto-grants-2000_12