HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442579Generated: October 30, 2026
Acetaldehyde → Methyl 4-cyano-2-(ethylamino)benzoate
https://huagongshe.com/reaction/1442579
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Benzoic acid, 2-amino-4-cyano-, methyl ester | HCID 10103677 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 4-cyano-2-(ethylamino)benzoate | HCID 23076867 | 23% |
Reaction Steps
Acetaldehyde (90%)(10 mL) and sodium triacetoxyborohydride (7.71 g, 36.4 mmol) were added to an acetic acid solution (10 mL) of methyl 2-amino-4-cyanobenzoate (3.04 g, 17.3 mmol) under ice cooling. The mixture was stirred at the same temperature for an hour and at room temperature for 2 hours. Ice water was added to the reaction mixture, the mixture was neutralized with sodium hydrogencarbonate, followed by extraction with ethyl acetate. The combined organic layers were washed with water and then saturated brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crystals obtained were washed with diisopropyl ether-hexane to give the title compound (800 mg, 23%). The residue was applied to silica gel column chromatography (hexane/ethyl acetate=50:1 and then 30:1). The crystals obtained were washed with hexane to give the title compound (920 mg, 26%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659267B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-74a073dbcb8f45c58f6674ad07984e17 |
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| Source note | uspto-grants-2010_02 |
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