3-BENZYLOXYANILINE CAS 1484-26-0

Introduction:Basic information about 3-BENZYLOXYANILINE CAS 1484-26-0, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

3-BENZYLOXYANILINE Basic information

Product Name:3-BENZYLOXYANILINE
Synonyms:Benzenamine, 3-(phenylmethoxy)-;M-(BENZYLOXY)ANILINE;3-BENZYLOXYANILINE;AKOS BBB/398;AKOS BC-2549;TIMTEC-BB SBB000388;3-Aminophenyl benzyl ether;3-Benzyloxyaniline 98%
CAS:1484-26-0
MF:C13H13NO
MW:199.25
EINECS:216-056-6
Product Categories:Anilines, Aromatic Amines and Nitro Compounds;Amines;C11 to C38;Nitrogen Compounds
Mol File:1484-26-0.mol

3-BENZYLOXYANILINE Chemical Properties

Melting point 63-67 °C (lit.)
Boiling point 170 °C(Press: 3 Torr)
density 1.129±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in Methanol
pka4.17±0.10(Predicted)
form Solid
color Pale brown
InChIInChI=1S/C13H13NO/c14-12-7-4-8-13(9-12)15-10-11-5-2-1-3-6-11/h1-9H,10,14H2
InChIKeyIGPFOKFDBICQMC-UHFFFAOYSA-N
SMILESC1(N)=CC=CC(OCC2=CC=CC=C2)=C1
CAS DataBase Reference1484-26-0(CAS DataBase Reference)
EPA Substance Registry System3-(Benzyloxy)aniline (1484-26-0)

Safety Information

Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
RIDADR 2811
WGK Germany 3
HazardClass IRRITANT
HS Code 29222990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3

3-BENZYLOXYANILINE Usage And Synthesis

Chemical PropertiesBeige to tan powder
Synthesis Reference(s)Tetrahedron Letters, 23, p. 147, 1982 DOI: 10.1016/S0040-4039(00)86770-2
Synthesis

24318-00-1

1484-26-0

591-27-5

Using 1-(benzyloxy)-3-nitrobenzene as the starting material, the reaction was carried out using an experimental method similar to that of Example 59, in which ferrous acetate (II), nickel nitrate (II), or cobalt acetylacetonate (III) was chosen as the metal reducing agent. The experimental results are detailed in Table 11. The data of Examples 60 to 66 show that the reaction rate is significantly enhanced when metal compounds such as iron, nickel or cobalt salts and amine additives such as pyrrolidine are added to the catalytic reduction system of the present invention in the presence of a rhodium/carrier catalyst. Under this condition, functional groups such as benzyl ether, which are easy to reduce, are retained, and nitro is selectively reduced to amino, thereby increasing the yield of the target products 3-benzyloxyaniline and 3-aminophenol.

References[1] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45
[2] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45
[3] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45
[4] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45
[5] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 45

3-BENZYLOXYANILINE Preparation Products And Raw materials

Raw materialsTetrahydrofuran-->Potassium carbonate-->Acetone-->Hydrogen-->Benzyl chloride-->4-Nitrophenol-->Rhodium-->Ferrous acetate-->1-(BENZYLOXY)-3-NITROBENZENE-->Pyrrolidine
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