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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21374Generated: October 26, 2026

Oxygen → (2R,3S)-N-(tert-Butyloxy)carbonyl-3-amino-2-acetoxy-4-phenylbutanal

https://huagongshe.com/reaction/21374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantDimethyl SulfideHCID 1068—
Reactant(3S,4S)-N-[(tert-Butyloxy)carbonyl]-4-amino-3-acetoxy-5-phenylpenteneHCID 10980116—
ReactantOxygen ozoneHCID 131711318—
SolventDichloromethaneHCID 6344—
Product(2R,3S)-N-(tert-Butyloxy)carbonyl-3-amino-2-acetoxy-4-phenylbutanalHCID 14856784—

Reaction Steps

Ozone/oxygen was bubbled at -70° C. into a solution of (3S,4S)-N-[(tert-Butyloxy)carbonyl]-4-amino-3-acetoxy-5-phenylpentene (2.55g, 8.0 mmol) [prepared by the method of Hanson et al., J. Ora. Chem., 50, 5399 (1985)] in 100 mL of methylene chloride until a deep blue color persisted. Oxygen was introduced until the blue color completely faded, then 3.0 mL of Me2S was added and the solution was allowed to warm to 0°-5° C. and stand overnight. The solvent was removed at 0° C. under vacuum yielding the title compound as a thick yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422349
Source datasetuspto-grants-1995_06
ORD IDord-8532a13b49be47c9ad77e4a04bda6575
Source noteuspto-grants-1995_06