Guanidine → HCID 58238472, compound

HRID 1961337Notes

Reaction equation

HRID 1961337 reaction equation
[CH2:1]([NH:5][CH3:6])[CH2:2][CH2:3][CH3:4].[CH:7]1([N:13]=[C:14]=[N:15][CH:16]2[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1.NC(N)=N>>[CH2:1]([N:5]([CH3:6])[C:14]([NH:13][CH:7]1[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]1)=[N:15][CH:16]1[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1)[CH2:2][CH2:3][CH3:4]

Participants

4

Reactant 3

HCID 3520GuanidineHCID 8068N-MethylbutylamineHCID 10868Dicyclohexylcarbodiimide2×

Product 1

HCID 58238472HCID 58238472, compound

Procedure

A mixture of 17.78 g of N-butyl-N-methylamine (0.204 mol) and 21.05 g of dicyclohexylcarbodiimide (0.102 mol) is refluxed for 3 h. GC analysis then shows a conversion of greater than 99.50 of the dicyclohexylcarbodiimide. The colorless final mixture is concentrated at 60° C. under 1 mbar for 2 h so as to give 29.9 g of a colorless and virtually odorless liquid of medium viscosity, corresponding to the expected guanidine (yield 99.70).

Workup

  1. temperatureis refluxed for 3 h
  2. concentrationThe colorless final mixture is concentrated at 60° C. under 1 mbar for 2 h so as
  3. customto give 29.9 g of a colorless and virtually odorless liquid of medium viscosity

Sources & evidence

ORD record
ord-54a0087be4dd42baad17417011ba66bd
Source dataset
uspto-grants-2013_04
Patent number
US08415018B2

Reaction notes

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