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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1589620Erstellt: 26. Oktober 2026

Pyridine → (4-Nitrophenyl)methyl 4-chloro-3-oxobutanoate

https://huagongshe.com/reaction/1589620

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt4-Nitrobenzyl alcoholHCID 69275—
Edukt4-Chloro-3-oxobutyryl chlorideHCID 3016262—
LösungsmittelDichloromethaneHCID 6344—
Produkt(4-Nitrophenyl)methyl 4-chloro-3-oxobutanoateHCID 20196963104,3%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04572801
Quelldatensatzuspto-grants-1986_02
ORD IDord-bd0e50e137d3417da7d549a5d1eba38e
Quellennotizuspto-grants-1986_02