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CAS RN: 132-16-1 | Product Number: P0774

Iron(II) Phthalocyanine


Purity: >97.0%(T)
Synonyms:
  • Phthalocyanine Iron(II)
Documents:
5G
€26.00
10   ≥20 
25G
€87.00
5   ≥20 

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Product Number P0774
Purity / Analysis Method >97.0%(T)
Molecular Formula / Molecular Weight C__3__2H__1__6FeN__8 = 568.38  
Physical State (20 deg.C) Solid
CAS RN 132-16-1
Reaxys Registry Number 15506728
PubChem Substance ID 87574915
SDBS (AIST Spectral DB) 5223
MDL Number

MFCD00015953

Specifications
Appearance Dark purple powder to crystal
Purity(Chelometric Titration) min. 97.0 %
Properties (reference)
GHS
Related Laws: / Compliance with laws, Regulations
Enzyme Commission 205-047-2
Transport Information:
HS Number 3204170090
Application
Catalytic Mitsunobu Reaction with an Iron Catalyst and Atmospheric Oxygen

Typical procedure: A mixture of ethyl L-(-)-lactate (100 mg, 0.85 mmol), 3,5-dinitrobenzoic acid (198 mg, 0.935 mmol), triphenylphosphine (446 mg, 1.7 mmol), ethyl 2-(3,4-dichlorophenyl)hydrazinecarboxylate (21.2 mg, 0.085 mmol), iron(II) phthalocyanine (48.3 mg, 0.085 mmol) and activated MS5Å (400 mg) in THF (1.7 mL) is heated at 65 °C for 24 h under air (balloon). After the reaction mixture is cooled to room temperature and filtered, the solvent is removed under reduced pressure. The residue is purified by silica gel chromatography (eluent: n-hexane/EtOAc = 6:1). Ethyl 2-(3,4-dichlorophenyl)azocarboxylate (20.1 mg, 0.0813 mmol, 96%) is recovered from the first fraction as a red solid. The second fraction gives (R)-1-ethoxycarbonylethyl 4-nitrobenzoate (209 mg, 0.668 mmol, 79%, 98:2 e.r.) as a white solid.

References


Application
Selective Nitro Reduction with an Iron-based Catalyst

Typical Procedure: Hydrazine hydrate (2 eq.) is added to a mixture of nitro compound (0.67 mmol) and catalyst (0.5 mol%) in water/ethanol (1:1) or ethylene glycol (10 mL). The reaction solution is refluxed to reflux at 120°C and the progress of the reaction is monitored by TLC (silica gel; hexane―ethyl acetate) and GC-MS. Upon completion, the reaction mixture is cooled to ambient temperature and extracted with ethyl acetate (3 × 5 mL). The combined organic fractions are (washed with water in cases where ethylene glycol is used as solvent) dried under reduced pressure. The product mixture is subjected to column chromatography (silica 230-400; hexane―ethyl acetate).

References


PubMed Literature


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