Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | HCID 131718515 | HCID 131718515 | — |
| Catalyst | HCID 23618985 | HCID 23618985 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 88428340 | HCID 88428340 | 76% |
Reaction Steps
The crude material of (2S,3S)-dimethyl-3-ethylaspartate hydrobromide (27.2 g) of Example 6 was suspended in water (200.0 mL) and filtered. The filter cake was washed with water (300.0 mL) 2nd the combined aqueous solution were diluted with methanol (500.0 mL). To this solution was added copper(II) carbonate copper(II) hydroxide (76.4 g, 345.5 mmol) and the resulting green suspension was mechanically stirred in a Morton flask (2.0 L) for 119 h. The suspension was saturated with hydrogen sulfide for 1 h, then the resulting black suspension was filtered through celite. The filter cake was washed with an aqueous solution of methanol (70%, 1800.0 mL). The combined filtrate and washings were concentrated in vacuo to give the amino acid salt (19.6 g) which was used for further reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05322942 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-b6378de493184479809213b7a4612b7e |
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| Source note | uspto-grants-1994_06 |
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