Acetic Anhydride → 1,1'-Thiobis(2,3-epithiopropane)

HRID 2206662

反応式

HRID 2206662 の反応式
ClCC(O)CSCC(O)CCl.[OH-].[Na+].NC(N)=S.C(OC(=O)C)(=O)C.O1CC1C[CH:28]1[S:40][CH:29]1[CH2:30][S:31][CH2:32][CH:33]1[S:39][CH:34]1CC1OC1>C1(C)C=CC=CC=1.CO>[S:39]1[CH2:34][CH:33]1[CH2:32][S:31][CH2:30][CH:29]1[S:40][CH2:28]1

参加物

8

反応条件

温度
36 °C

実験手順

1072.48 g (8.47 mol) of bis(3-chloro-2-hydroxypropyl)sulfide, 1300 g of toluene, and 800 g of methanol were put into a 10-liter reactor. The reaction temperature was adjusted to 30° C. with stirring. When the reaction temperature reached 25° C., NaOH (50% aq., 783.08 g, 9.78 mol) was added dropwise within 1 h. The reaction was carried out while maintaining a temperature of 35-37° C. After standing at 37° C. for about 30 min, 2000 g of toluene was added to the reaction mixture, followed by stirring for about 10 min. The resulting mixture was left standing for layer separation. The upper organic layer was washed twice with water, and then the water was removed as much as possible. To the organic layer was added 400 g of methanol. After stirring, thiourea (1117.65 g, 14.30 mol) and acetic anhydride (70 g) were added at a temperature of 8° C. The reaction was continued at 18° C. for 18 h. The reaction was stopped when almost all the starting materials disappeared, which was confirmed by HPLC, and the content of 2,3-epoxypropyl(2,3-epithiopropyl)sulfide reached 6%, which was confirmed by GC analysis. After completion of the reaction, stirring was stopped for layer separation. The obtained organic layer was washed three times with water and the organic solvent was removed, affording bis(2,3-epithiopropyl)sulfide. The product had a refractive index (nD, 20° C.) of 1.618.

後処理

  1. customwas adjusted to 30° C.
  2. customreached 25° C.
  3. stirringby stirring for about 10 min
  4. waitThe resulting mixture was left
  5. customstanding for layer separation
  6. washThe upper organic layer was washed twice with water
  7. customthe water was removed as much as possible
  8. additionTo the organic layer was added 400 g of methanol
  9. stirringAfter stirring
  10. waitThe reaction was continued at 18° C. for 18 h
  11. customAfter completion of the reaction
  12. stirringstirring
  13. customwas stopped for layer separation
  14. washThe obtained organic layer was washed three times with water
  15. customthe organic solvent was removed

出典と根拠

ORDレコード
ord-2a572ac447524c1f92b50e2165224176
出典データセット
uspto-grants-2016_06
特許番号
US09372281B2

関連ノート

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