HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604592Generated: October 27, 2026
Hydrochloric Acid → (S)-Benzyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate
https://huagongshe.com/reaction/604592
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-carbobenzyloxyalanine | HCID 736104 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-Benzyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate | HCID 10515879 | — |
Reaction Steps
CBZ-L-Alanine (6.5 kg, 28.5 mol), HOBT-hydrate (4.8 kg, 34.8 mol), N,O-dimethylhydroxylamine hydrochloride (3.4 kg, 36.2 mol) and THF (32 L) are charged to a clean flask under nitrogen. The mixture is cooled to 0-10° C. and then DIPEA (12.4 L) is slowly added at a temperature less than 20° C. EDC-HCl (7 Kg, 36.2 mol) is then added slowly with slight cooling at 15-25° C. The slurry is aged overnight at 20-25° C. The mixture is then cooled to 0-10° C. and 3 N HCl (13 L) is added slowly. Then IPAC (45.5 L) is added and the layers are separated. The organic layer is washed once with HCl (13 L) and twice with 8% NaHCO3 (13 L). The organic layer is then concentrated under vacuum to <20 L at 50° C. The clear solution is cooled slowly to room temperature, allowing the product to crystallize. Heptane (˜70 L) is then added slowly. The slurry is filtered, washed with heptane (18 L), and dried at room temperature on the filter pot. Product is obtained with >99.9% ee measured by chiral HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910592B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-dc6871c9f5b843619d1f390949df1926 |
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| Source note | uspto-grants-2011_03 |
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