HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Pyridine → (4-Nitrophenyl)methyl 4-chloro-3-oxobutanoate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | 4-Nitrobenzyl alcohol | HCID 69275 | — |
| Edukt | 4-Chloro-3-oxobutyryl chloride | HCID 3016262 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (4-Nitrophenyl)methyl 4-chloro-3-oxobutanoate | HCID 20196963 | 104,3% |
Reaktionsschritte
After 191.2 g (1.25 mol) of p-nitrobenzyl alcohol is dissolved in 250 ml of methylene chloride, 98.8 g of pyridine is added, and the mixture is cooled to -5° to 0° C. A solution of 193.75 g (1.25 mol) of γ-chloroacetoacetyl chloride (γ-CAC) in 431 ml of methylene chloride is added at the same temperature over an hour and, after completion of the addition, the mixture is stirred for 30 minutes. The resulting pyridine hydrochloride is filtered off. The filtrate and washings are combined and washed with 2 l-portions of water. The organic layer is dried over sodium sulfate and the solvent is then distilled off to give 354 g of p-nitrobenzyl γ-chloroacetoacetate as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04572801 |
| Quelldatensatz | uspto-grants-1986_02 |
| ORD ID | ord-bd0e50e137d3417da7d549a5d1eba38e |
| Quellennotiz | uspto-grants-1986_02 |