Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 86133272 | HCID 86133272 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,2'-Dithiodiethanesulfonic acid | HCID 65626 | 96% |
Reaction Steps
2,2′-Dithiobis ethane sulfonyl chloride (15.0 g, 47 mmol) was dissolved in a mixed solution of acetonitrile (100 mL) and water (30 mL). The reaction solution was stirred at room temperature for five days until no more sulfonyl chloride was detected. The reaction solution was then concentrated by rotary evaporation at elevated temperature to remove the volatile acetonitrile solvent and as much water as possible. The remaining aqueous solution was washed with dichloromethane (2×50 mL) and dried under high vacuum to give 12.7 g of disulfonic acid (96% yield). The product existed as a semi-solid form and was highly hygroscopic. It readily turned to a viscous liquid once exposed to air. No significant impurity was detected in the product by either NMR or HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07282602B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-13f2ea8d5f6f4b48aa0f88bffeb8dae7 |
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| Source note | uspto-grants-2007_10 |
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