HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099708Generated: October 25, 2026
Acetic Acid → [2-(3,4-Dimethoxy-phenyl)-1-methyl-ethyl]-ethyl amine
https://huagongshe.com/reaction/2099708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | 2-Propanone, 1-(3,4-dimethoxyphenyl)- | HCID 69896 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [2-(3,4-Dimethoxy-phenyl)-1-methyl-ethyl]-ethyl amine | HCID 22061570 | 92% |
Reaction Steps
A solution of 10 g (51.4 mmol) of 3,4-dimethoxyphenylacetone in 50 mL of methanol was cooled to 0° C. and was treated with 50 mL of 2M solution of ethylamine in methanol. To the reaction mixture 11.5 g (0.183 mmol) of sodium cyanoborohydride was added, and the pH of the reaction mixture was adjusted to 6.5-7 by adding glacial acetic acid. The mixture was allowed to stir at room temperature for 4 days. This was concentrated under reduced pressure, and 150 mL of water was added. The pH of the resulting solution was adjusted to 1 using 6 N HCl. This was extracted with 4×150 mL of ether and the organic layers were discarded. The pH of the aqueous layer was adjusted to 14, and the solution was extracted with 6×100 mL of chloroform. The organic layers were combined, dried (Na2SO4) and concentrated to dryness to give 10.6 g (47.4 mmol, 92%) of 2A as a pale yellow oil (M+H, 224).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569676B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-0fb2d5e7f40e4532b272da36311ba088 |
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| Source note | uspto-grants-2009_08 |
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