Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Ethylhexanoyl chloride | HCID 79103 | — |
| Solvent | Decane | HCID 15600 | — |
| Product | HCID 10916440 | HCID 10916440 | 93% |
Reaction Steps
Into a 200 ml beaker were charged 50 g of 1-hydroperoxy-1,3-dimethyl butyl peroxy-2-ethyl hexanoate (0.06 mole) in n-decane, 10 g of NaCl-25%, and 20 g of demi-water. The pH was adjusted with KOH-45% to 13.5 at a temperature of 8-12° C. Then 9.8 g of 2-ethylhexanoyl chloride were dosed in 20 minutes simultaneously with the lye, with the pH kept at >13.5. The mixture was stirred for another 60 minutes at 5-8° C. After separation of the water layer, the remaining hydroperoxide was reduced with a sulphite reduction. The organic layer was washed with NaHCO3-6%. The product was dried over magnesium sulphate. Yield: 47.4 g of product with an active oxygen content of 3.77% (chemical yield:93%). Ratio mono:bis=1:99.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552215B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-02208db0020e4d23b3c50c8d579fd63f |
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| Source note | uspto-grants-2003_04 |
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