HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434137Generated: October 27, 2026
Hydrochloric Acid → HCID 20610774, compound
https://huagongshe.com/reaction/434137
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | (S)-1-(p-tolyl)ethanamine | HCID 7015759 | — |
| Reactant | HCID 59119727 | HCID 59119727 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20610774 | HCID 20610774 | 85.6% |
Reaction Steps
(S)-3-Benzoyl-4-benzyloxycarbonylethyl-2,5-oxazolidinedione (L-N-benzoyl-O-benzylglutamic acid-NCA)(100 mg, 0.27 mmol) was dissolved in ethyl acetate (2.0 mL), followed by the addition of a solution of (S)-1-(p-tolyl)ethylamine (37 mg, 0.27 mmol) and N-methylmorpholine (28 mg, 0.27 mmol) in ethyl acetate (2.0 mL) at 0° C. The resulting mixture was stirred for 30 minutes. The reaction mixture was poured into 1 N hydrochloric acid (10 mL), followed by extraction with ethyl acetate (10 mL). The organic layer was washed successively with a saturated aqueous solution of sodium hydrogencarbonate (10 mL) and a saturated aqueous solution of sodium chloride (10 mL), and was then dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure to afford the title compound (106 mg, 85%) 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-6f5f015aa5f74002ada2b47c8301b4a5 |
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| Source note | uspto-grants-2003_12 |
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