HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995562Generated: October 31, 2026
Hydrochloric Acid → Methyl 2-amino-3-fluoro-2-(4-hydroxybenzyl)propanoate
https://huagongshe.com/reaction/1995562
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Amino-2-fluoromethyl-3-(4-hydroxyphenyl)propionic acid | HCID 11042087 | — |
| Product | Methyl 2-amino-3-fluoro-2-(4-hydroxybenzyl)propanoate | HCID 12768144 | 70% |
Reaction Steps
With ice cooling, a suspension of 2-amino-2-fluoromethyl-3-(4-hydroxyphenyl)propionic acid (10.0 g) in absolute methanol (400 ml, dried over magnesium) is saturated with HCl gas. After heating at 90° C. overnight, the solvent is removed under reduced pressure, and the residue is dried for 3 hours under the vacuum of an oil pump. After dissolving in absolute methanol (400 ml) and saturating with HCl gas, the mixture is heated at 90° C. overnight again. After evaporation of the solvent, the residue is dissolved in water and a solution of sodium carbonate is added with stirring until pH ~10. The suspension is extracted 3 times with ether; the combined ether extracts are filtered, washed carefully with water, dried (Na2SO4) and evaporated to give pure methyl-2-amino-2-fluoromethyl-3-(4-hydroxyphenyl)propionate (7.5 g, 70%) as white crystals, m.p. 130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04405530 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-604bfb3e667d46a2bb8541b5300878cf |
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| Source note | uspto-grants-1983_09 |
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