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

HRID 393895
ノート
印刷プレビュー

反応式

HRID 393895 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 784Hydrogen PeroxideHCID 6329MethylamineHCID 6348Carbon DisulfideHCID 14798Sodium Hydroxide

生成物 1

HCID 3034132{Disulfanediylbis[(sulfanylmethanylylidene)azanylylidene]}dimethane収率 97%

試薬・触媒・溶媒 4

HCID 176Acetic Acid溶媒
HCID 962
Water
溶媒
HCID 8028Tetrahydrofuran溶媒
HCID 8900Heptane溶媒

反応条件

温度
0 °C

実験手順

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.)

後処理

  1. customIn a 4-litter bottle equipped with a mechanical stirrer
  2. temperaturemaintained below 50° C.
  3. additionby adding ice
  4. stirringwith stirring
  5. stirringthe mixture was stirred for another 30 minutes in an ice-water bath
  6. filtrationThe mixture was filtered
  7. washwashed with aqueous trichloroacetic acid (2%, 5×200 mL) and hexanes (or heptane) (2×200 mL)
  8. customThe product was dried in air for 1 day to a constant weight
  9. customto give an off-white solid (205.8, yield: 97%)

出典と根拠

ORDレコード
ord-1b8aa46296514e0dbd5d520b30dabed2
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06809195B1

反応ノート

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