Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Mercaptoethansulphonic acid | HCID 14673438 | — |
| Reactant | Sodium mercaptoethanesulfonate | HCID 23690786 | — |
| Reactant | HCID 178418600 | HCID 178418600 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178418636 | HCID 178418636 | 98% |
Reaction Steps
12 g of sodium mercaptoethansulphonate are freed in aqueous solution and under nitrogen stream in a column, as described in the example 1. The mercaptoethansulphonic acid coming out of the column in aqueous solution, under nitrogen stream and at pH=1, is gradually added with arginine, in free base form, in stoichiometrical amount dissolved in water under nitrogen stream (12.7 g), by operating at pH values of between 6 and 7. Upon the salification is completed the pH of the solution of the salt must be of between 6 and 7. The solution is then concentrated to dryness giving a residue which, upon being taken with 200 ml of absolute ethanol, under stirring and in hot condition, is converted into white crystals. The suspension is agitated at 50° C. for 30 minutes, then cooled and filtered, whereby 22.8 g of white crystalline product are obtained, with a 98% yield and a melting point of 214°-216° C.; the pH in 10% aqueous solution is 6.7 and the solubility in water is perfect.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05019596 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-8fa67b1e6b1745b8aedca3a6d1c9500f |
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| Source note | uspto-grants-1991_05 |
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