2-Ethylhexanol → HCID 21806695, compound

HRID 1742769Notes

Reaction equation

HRID 1742769 reaction equation
Cl[C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4](C2C=CC=CC=2)[N:3]=1.ClC1C=C(Cl)N=CN=1.[CH2:23]([CH:25]([CH2:28][CH2:29][CH2:30][CH3:31])[CH2:26]O)[CH3:24]>CC(C)CCO>[Cl:8][C:6]1[N:5]=[CH:4][N:3]=[C:2]([CH2:26][CH:25]([CH2:23][CH3:24])[CH2:28][CH2:29][CH2:30][CH3:31])[CH:7]=1

Participants

5

Reactant 3

HCID 77202-EthylhexanolHCID 709434,6-DichloropyrimidineHCID 77338Fenclorim

Product 1

HCID 21806695HCID 21806695, compoundYield 76.2%

Reagents, catalysts & solvents 1

HCID 31260Isoamyl AlcoholSolvent

Procedure

The compound is prepared analogously to the method described in Example 3, with 4,6-dichloro-2-phenylpyrimidine being replaced by 4,6-dichloropyrimidine and 3-methylbutanol by 2-ethylhexanol. Yield: 76.2% of theory.

Workup

  1. customThe compound is prepared analogously to the method

Sources & evidence

ORD record
ord-64cf8c5d3e714c228dda8f46fc26eabe
Source dataset
uspto-grants-1994_08
Patent number
US05340701

Reaction notes

Loading…