Butylamine → HCID 178449173, compound
Reaction equation
[CH2:1]([NH2:5])[CH2:2][CH2:3][CH3:4].[CH:6]1([N:12]=[C:13]=[N:14][CH:15]2[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]2)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1>>[CH2:1]([NH:5][C:13]([NH:14][CH:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)=[N:12][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1)[CH2:2][CH2:3][CH3:4]Participants
3
Procedure
A mixture of 15.69 g of N-butylamine (0.214 mol) and 22.13 g of dicyclohexylcarbodiimide (0.107 mol) is heated at reflux for 2 h. GC analysis then shows a conversion of the dicyclohexylcarbodiimide of greater than 99.6%. The final colorless mixture is concentrated at 60° C. under 1 mbar for 2 h to give 29.7 g of a colorless, virtually odorless and moderately viscous liquid corresponding to the expected guanidine 2 (99% yield).
Workup
- temperatureis heated
- temperatureat reflux for 2 h
- concentrationThe final colorless mixture is concentrated at 60° C. under 1 mbar for 2 h
Sources & evidence
- ORD record
- ord-4693c0e579d94620970741d02ccecb0d
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08841372B2
Reaction notes
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