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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2405749Erstellt: 24. Oktober 2026

Acetanilide → HCID 54037375, Verbindung

https://huagongshe.com/de/reaction/2405749

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetanilideHCID 904—
EduktAcetic AnhydrideHCID 7918—
Edukt3-(4-Chloro-3-nitrophenyl)acrylic acidHCID 614919—
EduktTin atomHCID 5352426—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
ProduktHCID 54037375HCID 5403737595%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

Tin II chloride dihydrate (103 g, 0.46 mol) was dissolved in concentrated HCl (120 mL). Warming was necessary to obtain a clear solution. 4-Chloro-3-nitrocinnamic acid (25 g, 0.11 mol) was added portionwise with stirring. After about 20% of the starting material had been added, the mixture was warmed with a heat gun to 45° C. to initiate reaction. The rate of addition was controlled to maintain a temperature of 65-75° C. Cooling with a water bath was used to prevent the temperature exceeding 80° C. After the addition was complete and reaction started to subside, the mixture was transferred to an oil bath at 65° C. for 1 h. The mixture was cooled to room temperature. The solid was filtered, washed with 2 M HCl, (60 mL) and sucked dry. The filter cake was dried in a vacuum oven for 1 h, then in air overnight, to give about 34 g crude product. This material was suspended in acetic acid (100 mL) with stirring and acetic anhydride (100 mL, 1.1 mol) was added in one portion. The temperature rose to 35° C. After the initial exotherm subsided, the mixture was stirred in an oil bath at 110° C. for 2 h, but did not dissolve. LCMS showed complete conversion to the desired acetanilide. The solution was cooled and water (50 mL) was added cautiously. The mixture was concentrated to about 200 mL. More water (100 mL) and 2 M HCl (50 mL) were added. The precipitate was filtered, washed with water and dried to give 3-acetamido-4-chlorocinnamic acid (25.0 g, 95%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08809326B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-667423f988474931bbe12a074caff50d
Quellennotizuspto-grants-2014_08