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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1816002Erstellt: 26. Oktober 2026

Acryloyl chloride → 1-Acryloyl-3,4-dimethyl-5-phenylimidazolidin-2-one

https://huagongshe.com/reaction/1816002

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcryloyl chlorideHCID 13140—
EduktDiisopropylethylamineHCID 81531—
Edukt1,5-Dimethyl-4-phenylimidazolidin-2-oneHCID 230547—
KatalysatorCuprous chlorideHCID 62652—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Acryloyl-3,4-dimethyl-5-phenylimidazolidin-2-oneHCID 2289775878%

Reaktionsschritte

To a solution of (4 S, 5 R)1,5-dimethyl-4-phenyl-2-imidazolidinone (45.0 g, 237 mmole) and (i-Pr)2NEt (62 mL, 355 mmole) in CH2Cl2 (1200 mL) was added CuCl (50 mg, 0.51 mmole) then acryloyl chloride (29 mL, 355 mmole), and the mixture was heated to reflux. After 2 hr the mixture was cooled to RT, washed with H2O (3×400 mL), dried over MgSO4, and concentrated. The resulting solid was triturated with Et2O (300 mL) and collected by filtration to give the title compound (45.15 g, 78%): 1H NMR (300 MHz, CDCl3) δ 7.72 (dd, J=17.0, 10.5 Hz, 1 H), 7.20-7.38 (m, 3 H), 7.10-7.20 (m, 2 H), 6.40 (dd, J=17.0, 2.1 Hz, 1 H), 5.77 (dd, J=10.4, 2.0 Hz, 1 H), 5.36 (d, J=8.5 Hz, 1 H), 3.85-4.00 (m, 1 H), 2.85 (s, 3 H), 0.82 (d, J=6.6 Hz, 3 H); MS (ES) m/e 245 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06881736B1
Quelldatensatzuspto-grants-2005_04
ORD IDord-ff8a4e4761bb4141a29ac4fcb93da78c
Quellennotizuspto-grants-2005_04