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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 574039Erstellt: 25. Oktober 2026

Benzoyl chloride → Ethyl (1E)-N-benzoylethanimidate

https://huagongshe.com/reaction/574039

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktTriethylamineHCID 8471—
EduktEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
LösungsmittelTolueneHCID 1140—
ProduktEthyl (1E)-N-benzoylethanimidateHCID 1302860482%

Reaktionsschritte

First, 15.5 g of ethyl acetimidate hydrochloride, 150 mL of toluene, and 31.9 g of triethylamine (Et3N) were put into a 500-mL three-neck flask and stirred at room temperature for 10 minutes. With a 50-mL dropping funnel, a mixed solution of 17.7 g of benzoyl chloride and 30 mL of toluene were added dropwise to this mixture, and the mixture was stirred at room temperature for 24 hours. After a predetermined time elapsed, the reaction mixture was suction-filtered, and the solid was washed with toluene. The obtained filtrate was concentrated to give N-(1-ethoxyethylidene)benzamide (a red oily substance, 82% yield). A scheme of the synthesis of Step 1 is shown in the following (e-1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09034486B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-054ed1d128f9471588b200aa35f57463
Quellennotizuspto-grants-2015_05