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ChemicalBook CAS DataBase List 1-ETHYL-3-PHENYLUREA

1-ETHYL-3-PHENYLUREA synthesis

14synthesis methods
-

Yield:621-04-5 98%

Reaction Conditions:

in dichloromethane at 0 - 20; for 16 h;

Steps:

Step 1: 1-ethyl-3-phenylurea.

Prepared according to literature procedure. To stir a solution of ethylamine (676.05 μL, 12 mmol) in CH2Cl2 (44.0 mL) at 0 °C for 10 minutes was added slowly phenylisocyanate (1,100 μL, 10.1 mmol). The reaction mixture was stirred at 0 °C to room temperature for 16 hours to provide coloress mixture, washed with 2M HCl two times, then extracted with CH2Cl2. The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The white solid of 1-ethyl-3-phenylurea was obtained in 1,620 mg (98% yield). 1H NMR (300 MHz, CDCl3) δ 7.28 (d, J = 4.2 Hz, 3H), 7.10-7.02 (m, 1H), 6.91 (s, 1H), 5.16 (brs, 1H), 3.26 (q, J = 7.2 Hz, 2H), 1.71 (brs, 1H), 1.12 (t, J = 7.2 Hz, 3H). Other data was identical to the literature values.

References:

Duangjan, Chanikan;Rukachaisirikul, Vatcharin;Saithong, Saowanit;Kaeobamrung, Juthanat [Tetrahedron Letters,2018,vol. 59,# 39,p. 3537 - 3540] Location in patent:supporting information

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