HCID 788030, compound → HCID 178442913, compound

HRID 2163280Notes

Reaction equation

HRID 2163280 reaction equation
Cl.[Cl:2][C:3]1[CH:9]=[C:8]([Cl:10])[C:7]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])=[CH:6][C:4]=1[NH2:5].[Cl:30][C:31]1[CH:36]=[C:35]([Cl:37])[CH:34]=[C:33]([Cl:38])[C:32]=1[N:39]1[C:43](=[O:44])[CH2:42][C:41](OCC)=[N:40]1.ClC1C=C(Cl)C(OCCCCCCCCCCCCCCCC)=CC=1N>>[Cl:38][C:33]1[CH:34]=[C:35]([Cl:37])[CH:36]=[C:31]([Cl:30])[C:32]=1[N:39]1[C:43](=[O:44])[CH2:42][C:41]([NH:5][C:4]2[CH:6]=[C:7]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])[C:8]([Cl:10])=[CH:9][C:3]=2[Cl:2])=[N:40]1

Participants

4

Reactant 3

HCID 788030HCID 788030, compoundHCID 22753008HCID 22753008, compoundHCID 22753010HCID 22753010, compound

Product 1

HCID 178442913HCID 178442913, compound

Procedure

Using 18 g of 2,4-dichloro-5-octadecyloxyaniline hydrochloride and 13 g of 1-(2,4,6-trichlorophenyl)-3-ethoxy-2-pyrazolin-5-one, which were prepared in a manner similar to Steps (1) and (2) of Synthesis Example 1, similar procedures to Step (3) of Synthesis Example 1, were carried out and recrystallization was performed from 100 ml of ethanol to obtain 15 g of the desired coupler. The melting point thereof was 98 to 99° C.

Workup

  1. customrecrystallization
  2. customto obtain 15 g of the desired coupler
  3. customthereof was 98 to 99° C.

Sources & evidence

ORD record
ord-a92ff28b31974f28909647b4998059e3
Source dataset
uspto-grants-1979_01
Patent number
US04133686

Reaction notes

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