HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401870Generated: November 1, 2026
Benzylamine → (R)-N-Benzyl-2-acetamido-3-hydroxypropionamide
https://huagongshe.com/reaction/1401870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-Acetyl-D-serine | HCID 10844522 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-N-Benzyl-2-acetamido-3-hydroxypropionamide | HCID 10889901 | — |
Reaction Steps
4-methylmorpholine (7.3 ml) followed by isobutylchloroformate (12.35 ml) was added to a suspension of (R)-2-acetamido-3-hydroxypropanoic acid (7 grams) in tetrahydrofuran (147 ml) at −78 to −75° C., benzylamine (10.4 ml) was added to it and the reaction mixture temperature was raised to 30-35° C. then stirred for 30 minutes. The reaction mixture was filtered and the filtrate was distilled off under reduced pressure. The obtained residue was dissolved in methylene chloride (35 ml) and washed with aqueous hydrochloric acid followed by sodium carbonate and then with water. The solvent from the methylene chloride layer was distilled off completely under reduced pressure to get the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907132B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-9c2ebfb40b954fc9b72c201de48a8ff3 |
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| Source note | uspto-grants-2014_12 |
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