Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343746Generated: October 23, 2026

Carbon Dioxide → Methyl 6-amino-2-methyl-3-nitrobenzoate

https://huagongshe.com/en/reaction/343746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDimethyl SulfateHCID 6497—
ReactantSodium BicarbonateHCID 516892—
ReactantSodiumHCID 5360545—
Reactant6-Amino-2-methyl-3-nitrobenzoic acidHCID 15283172—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductMethyl 6-amino-2-methyl-3-nitrobenzoateHCID 15334532—

Reaction Steps

49.7 g (0.253 mol) of 2-methyl-3-nitro-6-aminobenzoic acid are dissolved in 380 ml of acetone and 43 g (0.51 mol) of sodium hydrogen carbonate are added. The mixture is then heated to boiling until evolution of CO2 is complete. 35.3 g (0.28 mol) of dimethyl sulfate are then added dropwise in the course of two hours at the boiling point of acetone to the suspension of the sodium salt of 2-methyl-3-nitro-6-aminobenzoic acid thus obtained, and the mixture is subsequently refluxed for a further three hours and then allowed to cool. After pouring the reaction mixture into 1.8 l of water, it is extracted with methylene chloride. After drying, the organic phase is concentrated. The solid obtained is sufficiently pure for the subsequent reaction (NMR). Yield: 50 g (0.238 mol)=94% of theory, m.p.: 92°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05863864
Source datasetuspto-grants-1999_01
ORD IDord-2969ee246e8847f390c9589c6bc88f54
Source noteuspto-grants-1999_01