HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037806Generated: November 2, 2026
Formic Acid → 5-[[Formyl(methyl)amino]methyl]-2-nitro-benzoic acid
https://huagongshe.com/reaction/1037806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | 5-(Methylaminomethyl)-2-nitro-benzoic acid | HCID 58018329 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[[Formyl(methyl)amino]methyl]-2-nitro-benzoic acid | HCID 58018326 | 87% |
Reaction Steps
To a 100 mL volume egg plant-shaped flask, there were added 4.0 mL of formic acid and 2.7 mL of acetic anhydride and the mixture was stirred at room temperature. Subsequent to this, 0.65 g of sodium formate and 5.58 g (content: 71.7 wt %) of 5-(N-methyl-aminomethyl)-2-nitrobenzoic acid were added to the foregoing mixture in two portions and then the resulting mixture was stirred at room temperature for one hour. After the confirmation of the progress of the reaction by HPLC, 32 mL of water was added thereto to separate out crystals and to form a slurry and then cooled to 9° C. and stirred overnight. The solid separated out of the reaction liquid was filtered off, washed with water, dried under reduced pressure to thus obtain 3.95 g of the title compound as a white crystalline solid (yield: 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546610B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-622c825af6174ca48d36310d00aa535a |
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| Source note | uspto-grants-2013_10 |
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