HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968429Generated: October 29, 2026
Acetic Acid → 2-[(4-Methoxybenzyl)amino]ethanol
https://huagongshe.com/reaction/968429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[(4-Methoxybenzyl)amino]ethanol | HCID 104469 | — |
Reaction Steps
Acetic acid (ca. 150 ml) was added to a solution of p-anisaldehyde (58.2 g, 0.42 mol) and ethanolamine (152 ml, 2.52 mol) in methanol (1 L), to achieve a pH of 6. Sodium triacetoxyborohydride (100 g, 0.47 mol) was added portionwise, and once addition was complete, the mixture was stirred at room temperature for 72 hours. The mixture was concentrated under reduced pressure, basified using 1N sodium hydroxide solution and extracted with dichloromethane (10×300 ml). The combined extracts were evaporated and the crude product was purified by column chromatography on silica gel using an elution gradient of dichloromethane:methanol (98:2 to 90:10) to afford the title compound, 42 g. 1H-NMR (CDCl3, 400 MHz) δ: 2.78 (t, 2H), 3.62 (t, 2H), 3.75 (m, 5H), 4.24 (s, 2H), 6.81 (d, 2H), 7.22 (d, 2H). LRMS: m/z (ES+) 182 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06958402B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-4f442d76abd44d09bdbf00f89fec27c9 |
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| Source note | uspto-grants-2005_10 |
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