HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589361Generated: November 1, 2026
Formic Acid → 3-Amino-3-(2-nitrophenyl)propionic acid
https://huagongshe.com/reaction/589361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Amino-3-(2-nitrophenyl)propionic acid | HCID 2779217 | 64.6% |
Reaction Steps
o-Nitrobenzaldehyde (20.4 g, 0.135 mol), formic acid (20.3 mL, 0.539 mol) and malonic acid (18.3 g, 0.176 mol) were stirred at 45° C. for half an hour. Then ammonium formate (21.3 g, 0.338 mol) was added thereto, the reaction temperature was raised to 70° C. and stirred for 1 hour, and then stirred at 95° C. for another 4 hours. Then concentrated hydrochloric acid (50 mL) was added and further stirred maintaining this temperature for another 1 hour. It was cooled. 25 mL water was added, and washed twice with ethyl acetate (2×25 mL). The aqueous phase was adjusted to pH 4.2 with 50% potassium hydroxide solution. A solid precipitated. It was pumping filtered, and dried in vacuum to obtain a yellow solid 18.33 g, at a yield of 64.6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233098B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-5b46d4276641465886391518d43599b7 |
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| Source note | uspto-grants-2016_01 |
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