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50609-01-3

50609-01-3 Structure

50609-01-3 Structure
IdentificationBack Directory
[Name]

4-(2-PYRROLIDIN-1-YL-ETHOXY)-PHENYLAMINE
[CAS]

50609-01-3
[Synonyms]

)ethoxy]aniL
4-[2-(1-PyrroL
4-(2-(Pyrrolidin-1-yl)
4-(2-Pyrrolidinoethoxy)aniline
4-(2-(PYRROLIDIN-1-YL)ETHOXY)ANILINE
4-(2-PYRROLIDIN-1-YL-ETHOXY)-PHENYLAMINE
BenzenaMine, 4-[2-(1-pyrrolidinyl)ethoxy]-
[Molecular Formula]

C12H18N2O
[MDL Number]

MFCD07790198
[MOL File]

50609-01-3.mol
[Molecular Weight]

206.28
Chemical PropertiesBack Directory
[Boiling point ]

362.2±22.0 °C(Predicted)
[density ]

1.097±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

9.76±0.20(Predicted)
[Appearance]

Light brown to brown Oil
[InChI]

InChI=1S/C12H18N2O/c13-11-3-5-12(6-4-11)15-10-9-14-7-1-2-8-14/h3-6H,1-2,7-10,13H2
[InChIKey]

OTYZNDKWNPQQJP-UHFFFAOYSA-N
[SMILES]

C1(N)=CC=C(OCCN2CCCC2)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Health Hazard (GHS08)Corrosion (GHS05)Environment (GHS09)Skull and Crossbones (GHS06)
GHS08,GHS05,GHS09,GHS06
[Signal word ]

Danger
[Hazard statements ]

H351-H318-H317-H400-H301-H341-H311-H331
[Precautionary statements ]

P273-P391-P501-P264-P270-P301+P310-P321-P330-P405-P501-P201-P202-P281-P308+P313-P405-P501-P280-P302+P352-P312-P322-P361-P363-P405-P501-P280-P305+P351+P338-P310-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P201-P202-P281-P308+P313-P405-P501-P261-P271-P304+P340-P311-P321-P403+P233-P405-P501
[HazardClass ]

IRRITANT
[HS Code ]

2921410090
Spectrum DetailBack Directory
[Spectrum Detail]

4-(2-PYRROLIDIN-1-YL-ETHOXY)-PHENYLAMINE(50609-01-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-(2-Pyrrolidin-1-ylethoxy)nitrobenzene

265654-77-1

4-(2-PYRROLIDIN-1-YL-ETHOXY)-PHENYLAMINE

50609-01-3

General procedure for the synthesis of 4-[2-(pyrrolidin-1-yl)ethoxy]aniline from 1-(2-(4-nitrophenoxy)ethyl)pyrrolidine: 1-[2-(4-nitrophenoxy)ethyl]pyrrolidine (purchased from CombiBlocks, LLC, 5.00 g, 0.0212 mol) was dissolved in 100 mL of methanol and 0.5 g of 10% Pd/C catalyst, and the hydrogenation reaction was carried out under a hydrogen atmosphere (using a balloon to provide hydrogen pressure) and the reaction continued overnight. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated to dryness, the resulting product was used directly in the next step of the reaction without further purification (Yield: 4.36 g, Yield: 99.88%). Spectral analysis of the product showed LCMS (M + H) 207.4.

[References]

[1] Patent: WO2009/64835, 2009, A1. Location in patent: Page/Page column 168
[2] Patent: WO2004/26823, 2004, A1. Location in patent: Page 36
[3] Patent: WO2016/34642, 2016, A1. Location in patent: Page/Page column 35
[4] Patent: US2015/336982, 2015, A1. Location in patent: Paragraph 0155; 0157
[5] Journal of Organic Chemistry, 1951, vol. 16, p. 1421,1424
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