Reaction #1672734
Related Literature (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US04436668
Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The procedure described in Example 4 is followed, but the n-pentanol and n-pentyl carbamate are replaced respectively by isoamyl alcohol and isoamyl carbamate, and diazabicyclo-[4,3,0]-nonene is used as the catalyst. After completion of the reaction, analysis by gas chromatography shows that 66.9% of isoamyl carbamate have been converted and 120.3 parts of diisoamyl carbonate (89% of theory, based on converted isoamyl carbamate), of boiling point 106°-108° C./18 mbar, have been formed. After completion of the reaction, analysis by gas chromatography
Source ID: ord-4bf290f41c1a4134b7f574cacdd973dc