Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 135773199 | HCID 135773199 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14091463 | HCID 14091463 | — |
Reaction Steps
A mixture of the product of step (b) (1.6 g; 4.8426 mmole) and diethyl oxalate (5.7 g; 39.041 mmole; 5.3 ml) in dry dimethylformamide (60 ml) was added slowly to a stirring suspension of ether washed sodium hydride (0.29 g; 12.0808 mmole) in dry dimethylformamide (10 ml) under nitrogen. After the addition, the mixture was allowed to stir for 7 hours. The reaction mixture was poured onto ice and was then acidified with dilute hydrochloric acid. The pH of the mixture was adjusted to about 6 before being extracted into chloroform. This was washed with water, dried and evaporated to give a yellow solid. The solid was taken up in ethanolic hydrogen chloride (50 ml) and heated to reflux on the steambath for 3 hours. The solution was cooled, treated with water and then concentrated. The pH of the mixture was adjusted to about 7 and then extracted into chloroform. The extract was washed with water, dried and evaporated, to give a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04419352 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-3a49a426ef224d1caf3b8db1f1afd594 |
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| Source note | uspto-grants-1983_12 |
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