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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456888Generated: October 25, 2026

Dimethyl Sulfide → 1-Benzyl-1,4,7,10-tetraazacyclododecane

https://huagongshe.com/reaction/1456888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
Reactant4-Benzyl-1,4,7,10-tetraazacyclododecane-2,6-dioneHCID 15702829—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-1,4,7,10-tetraazacyclododecaneHCID 10084082—

Reaction Steps

To a suspension of 890 mg (3.07 mmol) of 1-benzyl-3,11-dioxo-1,4,7,10-tetraazacyclododecane in tetrahydrofuran under nitrogen was added 2.64 ml of 8M borane-methyl sulfide complex (21.1 mol, 7 equivalents). The mixture was heated to reflux allowing the methyl sulfide to distill out of the reaction flask. After 2 hours, the reaction was quenched by the addition of 12 ml 1.8M hydrochloric acid in methanol and refluxed for an additional 3 hours. Volatiles were removed by evaporation, and the solid resuspended in methanol and reevaporated. The product was crystallized from methanol/ethyl acetate; yield 455 mg, 37%. Mass spectrum (CI): m/e 263 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846519
Source datasetuspto-grants-1998_12
ORD IDord-8e0dd062332042778c9c931619c142d1
Source noteuspto-grants-1998_12