HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655541Generated: October 31, 2026
Acetic Acid → (S)-4-(4-Hydroxy-butyl)-2-methyl-3-oxo-piperazine-1-carboxylic acid benzyl ester
https://huagongshe.com/reaction/655541
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Amino-1-butanol | HCID 25868 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | (S)-2-[Benzyloxycarbonyl-(2-oxo-ethyl)-amino]-propionic acid methyl ester | HCID 86638111 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-4-(4-Hydroxy-butyl)-2-methyl-3-oxo-piperazine-1-carboxylic acid benzyl ester | HCID 67079818 | 66% |
Reaction Steps
A solution of (S)-2-[benzyloxycarbonyl-(2-oxo-ethyl)-amino]-propionic acid methyl ester (24.3 g, 80 mmol) in dichloromethane (130 mL) was added at room temperature over 15 min to a suspension of 4-amino-1-butanol (7.12 g, 80 mmol), acetic acid (9.6 g, 0.16 mol), and sodium triacetoxyborohydride (25.4 g, 0.12 mol), then after 16 h triethylamine (16.2 g, 0.16 mol) was added, and the reaction mixture was concentrated under vacuum. The residue was partitioned between 2 M aq. sodium carbonate solution and ethyl acetate. The organic layer was dried (MgSO4), filtered, and evaporated. Chromatography (SiO2; dichloromethane, then dichloromethane/methanol/25% aq. ammonia solution 90:10:0.25) afforded the title compound (16.8 g, 66%). Yellow oil, MS (ISP)=321.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071586B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-b37f8927f5da450b8a9891e6cf63d7ba |
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| Source note | uspto-grants-2011_12 |
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