Hydrogen Peroxide → {Disulfanediylbis[(sulfanylmethanylylidene)azanylylidene]}dimethane
Reaction equation
[OH-].[Na+].[CH3:3][NH2:4].[C:5](=[S:7])=[S:6].OO>O.CCCCCCC.C(O)(=O)C.C1COCC1>[CH3:3][NH:4][C:5](=[S:7])[S:6][S:6][C:5](=[S:7])[NH:4][CH3:3]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 4
Conditions
- Temperature
- 0 °C
Procedure
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.)
Workup
- customIn a 4-litter bottle equipped with a mechanical stirrer
- temperaturemaintained below 50° C.
- additionby adding ice
- stirringwith stirring
- stirringthe mixture was stirred for another 30 minutes in an ice-water bath
- filtrationThe mixture was filtered
- washwashed with aqueous trichloroacetic acid (2%, 5×200 mL) and hexanes (or heptane) (2×200 mL)
- customThe product was dried in air for 1 day to a constant weight
- customto give an off-white solid (205.8, yield: 97%)
Sources & evidence
- ORD record
- ord-1b8aa46296514e0dbd5d520b30dabed2
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06809195B1
Reaction notes
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