Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Acetovanillone | HCID 2214 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | N-ethyl-3,4-epoxypyrrolidine | HCID 13320194 | — |
| Catalyst | Water | HCID 962 | — |
| Product | HCID 131714650 | HCID 131714650 | — |
Reaction Steps
A mixture of 17.0 g. (0.15 mole) of acetovanillone and 1-ethyl-3,4-epoxypyrrolidine and 3 drops of water was heated on a steam bath overnight. The mixture was dissolved in 250 ml. of methylene chloride and extracted with three 150-ml. portions of 5% sodium hydroxide and one 100-ml. portion of water. The methylene chloride layer wad dried over anhydrous sodium sulfate and concentrated to give 19.0 g. crude oil. This oil was chromatographed on 400 g. of silica gel. The desired product was eluted with acetone. The fractions were concentrated to give 14.0 g. of oil which was treated with oxalic acid in isopropyl alcohol. The resulting white solid was recrystllized twice from isopropyl alcohol to yield 13.4 g. (24%) of sesquioxalate, m.p. 121°-3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04585785 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-33f6449125e54105bca81b774c4b200d |
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| Source note | uspto-grants-1986_04 |
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