HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434138Generated: October 27, 2026
Hydrochloric Acid → HCID 20610770, compound
https://huagongshe.com/reaction/434138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (S)-1-(p-tolyl)ethanamine | HCID 7015759 | — |
| Reactant | HCID 45086078 | HCID 45086078 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20610770 | HCID 20610770 | 57% |
Reaction Steps
(S)-3-Acetyl-4-methyl-2,5-oxazolidinedione (N-acetyl-L-alanine-NCA)(424 mg, 2.7 mmol) was dissolved in ethyl acetate (10 mL), followed by the addition of (S)-1-(p-tolyl)ethylamine (406 mg, 3 mmol) at 0° C. The resulting mixture was stirred for 30 minutes. The reaction mixture was poured into 1 N hydrochloric acid (25 mL), followed by extraction with ethyl acetate (25 mL). The organic layer was washed successively with a saturated aqueous solution of sodium hydrogencarbonate (25 mL) and a saturated aqueous solution of sodium chloride (25 mL), and was then dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure, and the resulting white solid was washed with hexane-ethyl acetate to afford the title compound (380 mg, 57%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06670447B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-e5b1ae4ceafd475581a23e19078279e1 |
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| Source note | uspto-grants-2003_12 |
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