HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 54096093, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butyl ethyl malonate | HCID 96345 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 54096093 | HCID 54096093 | — |
Reaction Steps
This compound employed as the starting material in example 7 is prepared as follows: 10% NaOH (2 drops) is added to malonic acid tert-butyl ethyl ester (20 g). Aqueous 40% formaldehyde (15 ml) is then added very slowly thereto while keeping the temperature of the reaction mixture ≤5° C. and the pH at about 8.5 by means of 10% NaOH. The reaction mixture is then stirred at room temperature for 24 hours. The resulting reaction mixture is acidified by the addition of few drops of glacial acetic acid and charged, together with Cu(CH3COO)2, into a suitable distilling apparatus.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04914226 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-1eb20c620abc40459c6a25ae76a5b888 |
| Source note | uspto-grants-1990_04 |