HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655545Generated: October 26, 2026
Acetic Acid → (S)-4-(3-Hydroxymethyl-oxetan-3-ylmethyl)-2-methyl-3-oxo-piperazine-1-carboxylic acid benzyl ester
https://huagongshe.com/reaction/655545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | [3-(Aminomethyl)oxetan-3-yl]methanol | HCID 18706850 | — |
| Reactant | Sodium bis(acetyloxy)boranuidyl acetate | HCID 23676153 | — |
| Reactant | (S)-2-[Benzyloxycarbonyl-(2-oxo-ethyl)-amino]-propionic acid methyl ester | HCID 86638111 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-4-(3-Hydroxymethyl-oxetan-3-ylmethyl)-2-methyl-3-oxo-piperazine-1-carboxylic acid benzyl ester | HCID 67079867 | 14% |
Reaction Steps
A solution of (S)-2-[benzyloxycarbonyl-(2-oxo-ethyl)-amino]-propionic acid methyl ester (intermediate 27C; 258 mg, 0.92 mmol) in dichloromethane (1 mL) was added at room temperature to a suspension of (3-(aminomethyl)oxetan-3-yl)methanol (108 mg, 0.92 mmol), sodium triacetoxyborohyride (222 mg, 1.01 mmol) and acetic acid (111 mg, 1.85 mmol) in dichloromethane (1 mL). The reaction mixture was heated at 40° C. for 16 h, then partitioned between 1 M aq. sodium carbonate solution and ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated. The residue was taken up in methanol (2 mL), then after addition of potassium carbonate (255 mg, 1.85 mmol) the suspension was stirred for 2 h. The reaction mixture was partitioned between sat. aq. ammonium chloride solution and ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated. Chromatography (SiO2; dichloromethane/methanol/25% aq. ammonia solution 90:10:0.25) afforded the title compound (45 mg, 14%). Light yellow oil, MS (ISP)=349.3 (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-ed45d48a780f4bceb4db849b43d7bb90 |
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| Source note | uspto-grants-2011_12 |
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