HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508458Generated: October 30, 2026
Sulfuric Acid → (2S,5R)-benzyl 5-(benzyloxyamino)piperidine-2-carboxylate
https://huagongshe.com/reaction/508458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Phenylmethyl (2S)-5-[(phenylmethoxy)imino]-2-piperidinecarboxylate | HCID 86702281 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S,5R)-benzyl 5-(benzyloxyamino)piperidine-2-carboxylate | HCID 70673934 | 80% |
Reaction Steps
Under nitrogen atmosphere, tetrahydrofuran (2 ml) was added to (2S)-5-benzyloxyimino-piperidine-2-carboxylic acid benzyl ester (0.168 g, 0.50 mmol), and the mixture was cooled down to −10° C. Sulfuric acid (0.302 g, 3.06 mmol) was added to the mixture, and then sodium borohydride (0.0567 g, 1.50 mmol) was added. After 22 hours of stirring, the reaction mixture was analyzed with high performance liquid chromatography to find that the mixture contained 0.136 g of the title compound, and the reduction reaction proceeded with the yield of 80%. The diastereo selectivity was (2S,5R)/(2S,5S)=80.4/19.6 (60.8% de).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096523B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-7c4c08d5f923470a9f47d97d0bae6bb5 |
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| Source note | uspto-grants-2015_08 |
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