Sulfuric Acid → N-(2-cyclopropylethylidene)cyclohexylamine

Temperatur

0 °C

To a solution of cyclopropylacetonitrile (7.0 ml, 82 mmol) in 200 ml of methylene chloride/hexanes (1:1) at -78° C. was added 90.0 ml of 1M DIBAL in hexanes (90 mmol) dropwise over 20 minutes. After complete addition, the solution was warmed to 0° C. and stirred for 2 hours. At this time, 140 ml of ethyl acetate was added at 0° C. and the solution warmed to room temperature. To the solution was added 140 ml of saturated NH4Cl and 250 ml of 1N H2SO4. The mixture was diluted with ether and shaken vigorously until the organic layer became clear. The organic layer was then washed with saturated NaHCO3. To this crude aldehyde solution was added 55 g of K2CO3 and 9.4 ml of cyclohexylamine (82 mmol) at room temperature and the reaction stirred for 48 hours. The reaction was filtered and evaporated and the residue distilled under reduced pressure to give the title compound. MS 166 (M+H)+ ; 1H NMR (CDCl3) δ0.12-0.19 (m, 2H), 0.46-0.53 (m, 2H), 0.76-0.91 (m, 1H), 0.95-1.90 (m, 10H) , 2.12 (dd, 2H, J=5.2 Hz, J=7.4 Hz), 2.93 (m, 1H), 7.71 (t, 1H, J=5.1 Hz).

1. additionAfter complete addition
2. temperaturethe solution warmed to room temperature
3. stirringshaken vigorously until the organic layer
4. washThe organic layer was then washed with saturated NaHCO3
5. stirringthe reaction stirred for 48 hours
6. filtrationThe reaction was filtered
7. customevaporated
8. distillationthe residue distilled under reduced pressure

ORD-Eintrag

ord-5d7e661878ef46dba81c8c2cd4bbc194

Quelldatensatz

uspto-grants-1998_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05789591