HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470703Generated: October 27, 2026
Hydrogen Peroxide → Methyl 3-chloro-2-nitrobenzoate
https://huagongshe.com/reaction/1470703
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Benzoic acid, 2-amino-3-chloro-, methyl ester | HCID 11030511 | — |
| Catalyst | Tungstic acid | HCID 1152 | — |
| Catalyst | Tetradecyltrimethylammonium bromide | HCID 14250 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 3-chloro-2-nitrobenzoate | HCID 12187125 | 72% |
Reaction Steps
A solution of 7.1 g (28.5 mmol) of tungstic acid, 4.9 g (48.5 mmol) of concentrated sulfuric acid, 35.6 g (190 mmol) of methyl 2-amino-3-chlorobenzoate, and 5.84 g (20 mmol) of myristyltrimethylammonium bromide in 74 ml of toluene was heated to 47° C., and 50 ml (570 mmol) of a 35% hydrogen peroxide solution was added dropwise over 10 hours. The pH value at this time was 0.3. After the completion of the dropwise addition, the mixture was stirred at 47° C. for 4 hours. After the disappearance of the methyl 2-amino-3-chlorobenzoate was confirmed by HPLC analysis (area percentage method), 189.4 g (2.06 mol) of toluene and 19 g (150 mmol) of a 25% aqueous sodium hydroxide solution were added. The pH value at this time was 7.5. The reaction liquid was separated at 75° C., and 91 g of the aqueous layer was removed. Then, the obtained organic layer was cooled to 60° C. or less. 5.2 g (61.9 mmol) of sodium hydrogen carbonate and 5.2 ml of water were added, and 25 ml (285 mmol) of a 35% hydrogen peroxide solution was added dropwise while the reaction temperature was adjusted to 60° C. or less. After the completion of the dropwise addition, the mixture was stirred at 60° C. for 2 hours, and the reaction was completed. The reaction liquid was separated at room temperature. The obtained organic layer was analyzed by HPLC by the absolute calibration method, and as a result, the yield was 72%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006477B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-a0aa4fa263c84d4a9cd54b74665fdcf4 |
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| Source note | uspto-grants-2015_04 |
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