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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199874Generated: October 27, 2026

Sulfuric Acid → (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine

https://huagongshe.com/reaction/2199874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(2S)-5-[(benzyloxy)imino]-2-cyanopiperidineHCID 90088575—
SolventEthyl AcetateHCID 8857—
Product(2S)-5-[(benzyloxy)amino]-2-cyanopiperidineHCID 117599345—

Reaction Steps

The compound of Formula (IX) was reacted with sulphuric acid and sodium triacetoxy borohydride, in presence of suitable solvent such as ethyl acetate and at temperature below −5° C., to provide (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine (X). The compound of Formula (X) was purified by forming oxalate salt. The compound of Formula (X) was reacted with oxalic acid in a mixture of ethylacetate and acetone to provide (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine ethanedioate (1:1) (XI), which was further treated with sodium hydrogen carbonate to obtain purified (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine (XII). The racemic compound (XI) was treated with methanol to obtain pure (2S,5R)-5-[(benzyloxy)amino]-2-cyanopiperidine ethanedioate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359353B2
Source datasetuspto-grants-2016_06
ORD IDord-618ac040e7474dd4b15d7689665b0b6a
Source noteuspto-grants-2016_06