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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344025Generated: October 31, 2026

Oxygen → HCID 23225813, compound

https://huagongshe.com/reaction/344025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantDimethyl SulfideHCID 1068—
ReactantDichloromethaneHCID 6344—
ReactantN-t-Butoxycarbonyl-N-allyl-2,2-bis-phenyl-ethylamineHCID 54079479—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 23225813HCID 23225813—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Combine N-t-butoxycarbonyl-N-allyl-2,2-bis-phenyl-ethylamine (0.23 g, 0.68 mmol) and dichloromethane (10 mL) and methanol (0.5 mL). Cool the -78° C. Pass ozonized oxygen through the solution until a persistent light blue color is obtained. Pass nitrogen through the solution until the blue color dissipates. Add dimethyl sulfide (2.0 mL). Allow the reaction mixture to warm to ambient temperature and stir for 5.5 hours. Concentrate in vacuo to obtain a residue. Dilute the residue with ethyl acetate and extract with water. Separate the layers, dry the organic layer over MgSO4, filter, and evaporate in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864045
Source datasetuspto-grants-1999_01
ORD IDord-6daec64481d6447ba6c002f191517433
Source noteuspto-grants-1999_01