HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443046Generated: October 30, 2026
Epichlorohydrin → Tert-octylglycidyl thioether
https://huagongshe.com/reaction/443046
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | tert-OCTYL MERCAPTAN | HCID 8851 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-octylglycidyl thioether | HCID 85528098 | — |
Reaction Steps
A solution of 66 parts by weight of sodium hydroxide, 300 parts by weight of water and 8 parts by weight of tetrabutylammonium chloride is added dropwise at 15° to 20° C. in the course of 70 minutes, with stirring and partial cooling (especially at the commencement of the addition), to a mixture of 219 parts by weight of tert-octylmercaptan and 135 parts by weight of epichlorohydrin. The reaction mixture is further stirred for 1 hour at 50° C.; the aqueous phase is then separated, and the organic phase is washed with 200 parts by weight of water. The organic phase is finally distilled in vacuo to thus obtain the tert-octylglycidyl thioether in the form of a colourless liquid having a boiling point of 74° to 75° C. at 0.02 mbar, and a refractive index of nD20 =1.4803; the yield is 250 parts by weight, which corresponds to 82% of the theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05892051 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-8173d694907c48ed97bf5ac890961f27 |
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| Source note | uspto-grants-1999_04 |
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