Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylparaben | HCID 7456 | — |
| Reactant | Thietane, 1-oxide (9CI) | HCID 25747 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 21424533 | HCID 21424533 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23712208 | HCID 23712208 | — |
Reaction Steps
Sodium 3-(4-carbomethoxyphenoxy)propanesulfonate is prepared by adding sodium methoxide (54 grams) to 4-carbomethoxyphenol (152 grams) dissolved in 600 ml. of methanol followed by addition of propane sulfone (122 grams). After 2 hours of reflux, the crystals formed are filtered (186 grams) and added to tetra-n-butylphosphonium chloride (185 grams) in 400 ml. of water at 40° C. to prepare tetra-n-butylphosphonium 3-(4-carbomethoxyphenoxy)propanesulfonate. To remove this phosphonium salt from water, 70-ml. of chloroform is shaken with 70-ml. of the water solution and then separated from the water. This chloroform layer is then combined with the chloroform layer from a repeat of this procedure with 100-ml. of chloroform and a 100-ml. portion of the water solution. Evaporation of the combined chloroform extracts yields 98 g. of Salt E.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04035346 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-bf49107bc2e54d779cb457bb52a157bd |
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| Source note | uspto-grants-1977_07 |
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