Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl N-(2-ethoxy-2-oxoethyl)-N-formyl-beta-alaninate | HCID 281013 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53847768 | HCID 53847768 | — |
Reaction Steps
115.5 g of N-ethoxycarbonylethyl-N-formylglycine ethyl ester are dissolved in 150 ml of ethanol, and the solution is cooled to 0° C. To it is then added dropwise a mixture of 28.0 g of potassium hydroxide, 60 ml of water and 120 ml of ethanol. The reaction mixture is stirred for 18 h at RT, and is subsequently concentrated by evaporation under reduced pressure. After the addition of a small amount of water, the mixture is acidified with concentrated hydrochloric acid to pH 1. By extraction with chloroform, drying, and concentration of the organic phase by evaporation,there is obtained N-ethoxycarbonylethyl-N-formylglycine in the form of a yellowish oil (compound No. 1.3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04868202 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-7e5804b3fd744e03a8404d5342d2e30b |
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| Source note | uspto-grants-1989_09 |
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