HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508452Generated: October 30, 2026
Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- → (2S,5R)-benzyl 5-(benzyloxyamino)piperidine-2-carboxylate
https://huagongshe.com/reaction/508452
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| 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 | 82.3% |
Reaction Steps
Under nitrogen atmosphere, (±)-camphorsulfonic acid (0.697 g, 3.00 mmol) and tetrahydrofuran (2 ml) was added to (2S)-5-benzyloxyimino-piperidine-2-carboxylic acid benzyl ester (0.169 g, 0.50 mmol), and the mixture was cooled down to −20° C. Borane-tetrahydrofuran complex (1.06 M tetrahydrofuran solution, 2.4 ml, 2.54 mmol) was added to the mixture for 1.5 hours, and the obtained mixture was stirred for 6 hours. The reaction mixture was analyzed with high performance liquid chromatography to find that the reaction mixture contained 0.140 g of the title compound, and the reduction reaction proceeded with yield of 82%. The diastereo selectivity was (2S,5R)/(2S,5S)=87.8/12.2 (75.6% 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-06368c262d864600b0d9fc8a31bcdfaa |
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| Source note | uspto-grants-2015_08 |
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