Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methylglyoxal | HCID 880 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | (Tetrahydrofuran-3-yl)hydrazine hydrochloride | HCID 19432761 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66920530 | HCID 66920530 | 53% |
Reaction Steps
Acetic acid (1.7 mL) was slowly added to a solution of tetrahydrofuran-3-ylhydrazine hydrochloride (2.50 g, 18.0 mmol) (prepared as described by Bacon, E. R.; Singh, B.; and Lesher, G. Y. in U.S. Pat. No. 5,294,612) in water (30 mL). This mixture was then added dropwise to a solution of pyruvaldehyde (2.59 g, 2.34 mL, 14.4 mmol) in water (240 mL). The mixture was stirred overnight at room temperature. The mixture was poured into a seperatory funnel, NaCl was added and dissolved in the aqueous phase and then extracted with CH2Cl2 (6-times). The combined organic extracts were dried over Na2SO4, filtered and concentrated to provide crude material, which was purified by preadsorbing the oil on SiO2 followed by chromatography (Isco, 80 g RediSep column) eluting with a 0-80% EtOAc/heptane gradient over 80 minutes. Analysis of fractions resulted in isolation of 2-oxopropanal tetrahydrofuran-3-ylhydrazone (1.19 g, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318762B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-c0b42638945343b8864f0e1d528c697f |
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| Source note | uspto-grants-2012_11 |
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