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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium borohydrideHCID 4311764—
ReactantPhenylmethyl (2S)-5-[(phenylmethoxy)imino]-2-piperidinecarboxylateHCID 86702281—
SolventTetrahydrofuranHCID 8028—
Product(2S,5R)-benzyl 5-(benzyloxyamino)piperidine-2-carboxylateHCID 7067393480%

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096523B2
Source datasetuspto-grants-2015_08
ORD IDord-7c4c08d5f923470a9f47d97d0bae6bb5
Source noteuspto-grants-2015_08