Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyruvic Acid | HCID 1060 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (Ethylsulfanyl)(iodomethoxy)methanone | HCID 11436522 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14800951 | HCID 14800951 | — |
Reaction Steps
Redistilled 2-oxopropanoic acid (12.6 ml, 0.18 mol) is added to a vigorously stirred mixture of NaHCO3 (30.6 g, 0.36 mol), TBA HSO4 (61.2 g, 0.18 mol), H2O (360 mL), and CH2Cl2 (360 mL) in an open Erlenmeyer flask. Following stirring for 10 min 5b (44.0 g, 0.18 mol) in CH2Cl2 (400 mL) is added during 3 h at 25° C. together with CH2Cl2 (500 mL) in portions to compensate for the evaporation. In this way the formation of sulfurous by-products is minimized. The mixture is extracted with CH2Cl2 (300-200 mL). The combined organic phases are washed with H2O (2×200 mL); dried (MgSO4) and evaporated. The residue is triturated with Et2O (600 mL). After filtration the filtrate is treated with charcoal, evaporated, and the residue crystallized from pentane at -70° C. to yield 6ob, melting below room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05401868 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-cdd9133e3343403ca5563e14815322e7 |
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| Source note | uspto-grants-1995_03 |
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