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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantPhenylmethyl (2S)-5-[(phenylmethoxy)imino]-2-piperidinecarboxylateHCID 86702281—
SolventTetrahydrofuranHCID 8028—
Product(2S,5R)-benzyl 5-(benzyloxyamino)piperidine-2-carboxylateHCID 7067393482.3%

Reaction Conditions

Temperature-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096523B2
Source datasetuspto-grants-2015_08
ORD IDord-06368c262d864600b0d9fc8a31bcdfaa
Source noteuspto-grants-2015_08