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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1252217Erstellt: 27. Oktober 2026

4-Nitrobenzyl alcohol → p-Nitrobenzyl 4-p-methoxybenzyloxycarbonyl-4-methylvalerate

https://huagongshe.com/reaction/1252217

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Nitrobenzyl alcoholHCID 69275—
Edukt4-Methyloxybenzyl chlorideHCID 69993—
EduktDihydro-3,3-dimethyl-2H-pyran-2,6(3H)-dioneHCID 76247—
Eduktp-Nitrobenzyl 4-carboxy-4-methylvalerateHCID 20140795—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTriethylamineHCID 8471—
Produktp-Nitrobenzyl 4-p-methoxybenzyloxycarbonyl-4-methylvalerateHCID 20140840—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of p-nitrobenzyl 4-carboxy-4-methylvalerate (17.26 g) in dry dimethylformamide (100 ml), prepared by the procedure similar to that described in Example 174 from 2,2-dimethylglutaric anhydride and p-nitrobenzyl alcohol, was added p-methoxybenzyl chloride (9.16 g) and triethylamine (5.91 g). The reaction mixture was stirred at 80° C. for 9.5 hours, diluted with water and extracted with diethyl ether. The extract was washed successively with aqueous potassium carbonate, water, dilute hydrochloric acid and again water, dried over anhydrous sodium sulfate and evaporated to give p-nitrobenzyl 4-p-methoxybenzyloxycarbonyl-4-methylvalerate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04742052
Quelldatensatzuspto-grants-1988_05
ORD IDord-2bae3c7b3497440ab93648332a424e42
Quellennotizuspto-grants-1988_05