HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442549Generated: October 26, 2026
Formaldehyde → Methyl 2-dimethylamino-3-benzoylphenylacetate
https://huagongshe.com/reaction/442549
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl 2-amino-3-benzoylphenylacetate | HCID 12901250 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-dimethylamino-3-benzoylphenylacetate | HCID 12901251 | — |
Reaction Steps
A stirred solution of 4.6 gms. (0.0165 mole) of methyl 2-amino-3-benzoylphenylacetate and 13.2 ml. (0.165 mole) of 37% formaldehyde in 66 ml. of acetonitrile was treated wih 3.14 gms. (0.0495 mole) of sodium cyanoborohydride. Glacial acetic acid (1.65 ml.) was added over a ten minute period and stirring contained for 2.0 hrs. at room temperature. An additional 1.65 L ml. of glacial acetic acid was added and the mixture stirred over a weekend (co. 65 hours). The mixture was diluted with ether and the ether solution was successively washed with 3N potassium hydroxide solution, water, dried over sodium sulfate and concentrated under vacuum to give approximately 1.0 g. (18%) of a yellow oil. A portion of the oil was molecularly distilled for an analytical sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04045576 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-bc9c1c6aa46e425bab1573b40eec66e0 |
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| Source note | uspto-grants-1977_08 |
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