HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58863Generated: October 29, 2026
Glycine → 2-Amino-3-hydroxy-3-(4-methoxyphenyl)propanoic acid
https://huagongshe.com/reaction/58863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-3-hydroxy-3-(4-methoxyphenyl)propanoic acid | HCID 15594562 | 23% |
Reaction Steps
A solution of glycine (45 g, 0.60 mol) and anisaldehyde (122 g, 0.900 mol) in ethanol (1.5 L) was stirred at ambient temperature and KOH (82.7 g, 1.47 mol) was added. The reaction mixture was stirred overnight at ambient temperature. The mixture was concentrated under vacuum the majority of ethanol. The residue was dissolved in water (800 mL) and the solution was adjusted to pH=5 with 4 N aqueous HCl. The resulting mixture was washed with EtOAc (200 mL×2) to remove any impurities. The aqueous layer was concentrated to a volume of ˜400 mL. The mixture was filtered and the filtration cake was washed thoroughly with water (100 mL×2) and dried to afford 2-amino-3-hydroxy-3-(4-methoxyphenyl)propanoic acid (29 g, 23% yield, threo-) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434761B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-b504646607eb44c2a4a30f3f99ae848a |
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| Source note | uspto-grants-2016_09 |
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