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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 6-Amino-2-methyl-3-nitrobenzoic acid | HCID 15283172 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 6-amino-2-methyl-3-nitrobenzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05863864 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-2969ee246e8847f390c9589c6bc88f54 |
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| Source note | uspto-grants-1999_01 |
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