Methylamine → N-methyl bromomaleimide

温度

60 °C

Pursuant to steps a and b of Reaction Scheme 14, a solution of bromomaleic anhydride (52.8 g, 0.298 mol) in diethyl ether (250 mL) was cooled to 5° C. A 2 M solution of methylamine in THF (298 mL, 0.596 mol, 2 eq.) was added dropwise over 1 hour and the reaction stirred for a further 30 minutes, maintaining the temperature below 10° C. The resulting precipitate was filtered, washed with diethyl ether (2×100 mL) and air-dried for 30 minutes, then suspended in acetic anhydride (368 mL) and sodium acetate (12.2 g, 0.149 mol, 0.5 eq.) added. The reaction was heated to 60° C. for 2 hours and solvent was then removed in vacuo. The residue was taken up in DCM (500 mL) and washed with saturated sodium bicarbonate solution (2×500 mL) and water (2×300 mL). Organics were dried over MgSO4 (89 g), filtered and reduced in vacuo. The resulting oil was azeotroped with toluene (4×100 mL) to give N-methyl bromomaleimide as a beige solid. Yield=41.4 g (73%); 1H NMR (300 MHz, CDCl3) δ 6.95 (1H, s, CH), 3.07 (3H, s, NCH3).

1. customPursuant to steps a and b of Reaction Scheme 14
2. temperaturemaintaining the temperature below 10° C
3. filtrationThe resulting precipitate was filtered
4. washwashed with diethyl ether (2×100 mL)
5. customair-dried for 30 minutes
6. customsolvent was then removed in vacuo
7. washwashed with saturated sodium bicarbonate solution (2×500 mL) and water (2×300 mL)
8. dry with materialOrganics were dried over MgSO4 (89 g)
9. filtrationfiltered
10. customThe resulting oil was azeotroped with toluene (4×100 mL)

ORDレコード

ord-76fc776ec2154b97ae2cb2b9b7a42be3

出典データセット

uspto-grants-2014_11

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08877798B2