Epichlorohydrin → HCID 12520694, compound

HRID 2106906Notes

Reaction equation

HRID 2106906 reaction equation
[CH2:1]([SH:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:10]([CH:12]1[O:14][CH2:13]1)Cl>[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.[OH-].[Na+]>[CH2:1]([S:9][CH2:10][CH:12]1[O:14][CH2:13]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

Participants

5

Procedure

293 g of n-octylmercaptan and 5 g of tetrabutylammonium chloride are placed into a 1 liter Sovirel reactor (double-walled reaction vessel) fitted with thermometer, stirrer, dropping funnel, dosing dropping-funnel and pH-electrode. To this solution are added dropwise within 80 minutes at a pH value of 11.6-12.0, with stirring and intensive cooling, 184 g of epichlorohydrin. The pH value is maintained constant over the total period of 80 minutes by the corresponding controlled addition of about 10 ml of a 22% aqueous sodium hydroxide solution. The reaction temperature should not exceed 20° C. After completion of the exothermic reaction, 305 ml of 22% sodium hydroxide solution are introduced dropwise within 15 minutes. The reaction mixtue is subsequently stirred at 50° C. for 30 minutes; the aqueous phase is then separated, the organic phase is washed twice with 200 g of water each time, and the organic phase is fractionated in vacuo. The yield is 382 g (94% of theory) with a boiling point of 92°-94° C. at 0.04 mbar and a refractive index of nD20 : 1.4718.

Workup

  1. customfitted with thermometer, stirrer
  2. additionTo this solution are added dropwise within 80 minutes at a pH value of 11.6-12.0
  3. customexceed 20° C
  4. additionare introduced dropwise within 15 minutes
  5. stirringThe reaction mixtue is subsequently stirred at 50° C. for 30 minutes
  6. customthe aqueous phase is then separated
  7. washthe organic phase is washed twice with 200 g of water each time

Sources & evidence

ORD record
ord-2002a0dc1cff4c04aa988b968fd6a530
Source dataset
uspto-grants-1990_06
Patent number
US04931576

Reaction notes

Loading…