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

Temperatur

36 °C

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 14%, 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 1.611.

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

ORD-Eintrag

ord-7a64d79ea6894a619dd23c2f250c386a

Quelldatensatz

uspto-grants-2016_06

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09372281B2