HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548611Generated: October 30, 2026
Ethanolamine → 2-[(4-Methoxybenzyl)amino]ethanol
https://huagongshe.com/reaction/548611
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-[(4-Methoxybenzyl)amino]ethanol | HCID 104469 | — |
Reaction Steps
A 1 L round bottom flask is charged with 2-aminoethanol (29 g, 213 mmol), 4-methoxybenzaldehyde (39 g, 639 mmol), methanol (250 mL) and acetic acid (75 mL) under a nitrogen atmosphere. The contents were cooled to 0° C. and sodium triacetoxyborohydride (50 g, 234 mmol) was added over a 20 minute period. The reaction mixture was stirred at room temperature for 18 hours, concentrated under reduced pressure and partitioned between water (500 mL) and ethyl acetate (500 mL). The ethyl acetate layer was washed with 3N HCl (400 mL). The HCl layer is separated, cooled to 0° C., made basic using 6N NaOH and extracted with dichloromethane (2×100 mL). The dichloromethane layer was dried over sodium sulfate and concentrated under reduced pressure to yield the title compound a as an oil (20 g). 1H-NMR of the oil was consistent with the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943617B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-7a31ab6623104d0e8851f93e9c4dfdd3 |
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| Source note | uspto-grants-2011_05 |
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