반응 #2042677

ord-71ee16c1c3fc40adbe415da44ff31e07

반응 방정식

CSc1ccc(C(=O)C(C)(C)N2CCOCC2)cc1
2-methyl-1-(4-methylthiophenyl)-2-morpholino-1-propanone
C=C[Si](OC)(OC)OC
vinyltrimethoxysilane
CO[Si](CCc1cc(SC)ccc1C(=O)C(C)(C)N1CCOCC1)(OC)OC
yellowish oil
수율 54.7%
CO[Si](CCc1cc(SC)ccc1C(=O)C(C)(C)N1CCOCC1)(OC)OC
2-methyl-1-[4-methylthio-2-(2-trimethoxysilylethyl)phenyl]-2-morpholino-1-propanone
수율 54.7%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 5 hours
  2. 2
    workup.WAITboiling was repeated for 4 hours
  3. 3
    온도at reflux for a further 5 hours
  4. 4
    농축Concentration and chromatography (silica gel, CH2Cl2 /ethyl acetate)

실험 절차

11.18 g (40 mmol) of 2-methyl-1-(4-methylthiophenyl)-2-morpholino-1-propanone, 735 mg (0.8 mmol) of RuH2 (CO)(PPh3)3 and 7.3 ml (48 mmol) of vinyltr 60 ml of anhydrous toluene were degased with argon for 1/2 hour and boiled at reflux for 5 hours. After standing overnight, boiling was repeated for 4 hours, then 360 mg (0.4 mmol) of RuH2 (CO)(PPh3)3 and 2 ml (13 mmol) of vinyltrimethoxysilane were added, and the mixture was stirred at reflux for a further 5 hours. Concentration and chromatography (silica gel, CH2Cl2 /ethyl acetate) gave 3.04 g (18%) of a yellowish oil. 1H-NMR (CDCl3): 1.01 ppm (2H, mc, Et-H2); 1.22 ppm (6H, s, Pr-H3, CH3); 2.50 ppm (3H, s, -SCH3); 2.58 ppm (4H, mc, *morpholine--O--CH2); 2.69 ppm (2H, mc, Et-H1); 3.59 ppm (9H, s, Si(OCH3)3); 3.70 ppm (4H, mc, **morpholine--N--CH2); 7.03 ppm (1H, dd, Ph-H5, 3 JH5, H6 =8.4 Hz, 4JH3,h5 =2.0 Hz); 7.11 ppm (1H, d, Ph-H3); 8.47 ppm (1H, d, Ph-H6).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05776658uspto-grants-1998_07