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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1252225Erstellt: 27. Oktober 2026

Triethylamine → 4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol

https://huagongshe.com/reaction/1252225

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
Edukt4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acidHCID 13334384—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanolHCID 20140800—

Reaktionsschritte

To a mixture of 4-methyl-4-(p-nitrobenzyloxycarbonyl)aminovaleric acid (14.0 g) and triethylamine (5.25 g) in tetrahydrofuran (280 ml), ethyl chloroformate (5.64 g) was added with ice-cooling and then stirred for 30 minutes. The resulting triethylamine hydrochloride was removed by filtration. To filtrate was added sodium borohydride (5 g) in water (90 mg) with ice-cooling, and the mixture was stirred for 1.5 hours. The reaction mixture was concentrated to a volume of 120 ml in vacuo and extracted with dichloromethane. The dichloromethane layer was washed with diluted hydrochloric acid and then water, dried over anhydrous sodium sulfate and evaporated in vacuo to give an oily residue which was then purified by silica gel chromatography to give 4-methyl-4-(p-nitrobenzyloxycarbonyl)aminopentanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04742052
Quelldatensatzuspto-grants-1988_05
ORD IDord-aeb5bb4dba7b42c5bfeaebee6c17486c
Quellennotizuspto-grants-1988_05