3-[2-(3-Formylphenoxy)ethoxy]benzaldehyde → HCID 178478834, compound

HRID 377035Notes

Reaction equation

HRID 377035 reaction equation
[CH2:1]([CH2:11][O:12][C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=1)[CH:16]=O)[O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]=O.[C:21]([NH:24][NH2:25])([NH2:23])=[NH:22].[ClH:26]>C(O)C.Cl.Cl.NNC(N)=N>[ClH:26].[ClH:26].[C:21]([NH:24][N:25]=[CH:6][C:5]1[CH:8]=[CH:9][CH:10]=[C:3]([O:2][CH2:1][CH2:11][O:12][C:13]2[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=2)[CH:16]=[N:25][NH:24][C:21](=[NH:22])[NH2:23])[CH:4]=1)(=[NH:23])[NH2:22]

Participants

5

Reactant 2

HCID 45636613-[2-(3-Formylphenoxy)ethoxy]benzaldehydeHCID 178418668HCID 178418668, compound

Product 1

HCID 178478834HCID 178478834, compoundYield 78.5%

Reagents, catalysts & solvents 2

HCID 178478830HCID 178478830, compoundCatalystHCID 702EthanolSolvent

Procedure

3,3'-(ethylenedioxy)dibenzaldehyde (1.08 g), aminoguanidine hydrochloride (1.105 g), and aminoguanidine dihydrochloride (0.005 g) were heated in 96% ethanol (6.25 mL) for 18 hr under nitrogen. Cooling and filtration gave 1.428 g of 3,3'-(ethylenedioxy)dibenzaldehyde bis(amidinohydrazone) dihydrochloride, mp 264-6° C.

Workup

  1. temperatureCooling
  2. filtrationfiltration

Sources & evidence

ORD record
ord-57ee2eb18be54abebacd17a7b2f76237
Source dataset
uspto-grants-2000_02
Patent number
US06022900

Reaction notes

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