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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393895Generated: October 30, 2026

Hydrogen Peroxide → {Disulfanediylbis[(sulfanylmethanylylidene)azanylylidene]}dimethane

https://huagongshe.com/reaction/393895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantMethylamineHCID 6329—
ReactantCarbon DisulfideHCID 6348—
ReactantSodium HydroxideHCID 14798—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHeptaneHCID 8900—
Product{Disulfanediylbis[(sulfanylmethanylylidene)azanylylidene]}dimethaneHCID 303413297%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 4-litter bottle equipped with a mechanical stirrer, sodium hydroxide (80 g, 2 mol) was dissolved in water (500 mL) and the solution was cooled to 0° C. (ice-water bath). THF (200 mL), methylamine (40% in water, 170 mL, 2 mol) and carbon disulfide (120 mL, 2 mol) were added and the mixture as stirred at 0° C. for 30 minutes. Crushed ice (1.5 kg) was added, followed by glacial acetic acid (300 mL). Hydrogen peroxide (30%, 100 mL, 1 mol) was added dropwise over 10 minutes with temperature maintained below 50° C. by adding ice with stirring. Hexanes (or heptane) (800 mL) was added and the mixture was stirred for another 30 minutes in an ice-water bath. The mixture was filtered and washed with aqueous trichloroacetic acid (2%, 5×200 mL) and hexanes (or heptane) (2×200 mL). The product was dried in air for 1 day to a constant weight to give an off-white solid (205.8, yield: 97%). M.p. 98-100° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809195B1
Source datasetuspto-grants-2004_10
ORD IDord-1b8aa46296514e0dbd5d520b30dabed2
Source noteuspto-grants-2004_10